SNP Links for Gene (Select 6564) - SNP

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Select item 14915872821.

rs1491587282 has merged into rs4646233 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAA>-,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:98684551 (GRCh38)
13:99336805 (GRCh37)
Canonical SPDI:: NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98684545:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SLC15A1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
AAA=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.98684551_98684568del, NC_000013.11:g.98684556_98684568del, NC_000013.11:g.98684557_98684568del, NC_000013.11:g.98684558_98684568del, NC_000013.11:g.98684559_98684568del, NC_000013.11:g.98684560_98684568del, NC_000013.11:g.98684562_98684568del, NC_000013.11:g.98684563_98684568del, NC_000013.11:g.98684564_98684568del, NC_000013.11:g.98684565_98684568del, NC_000013.11:g.98684566_98684568del, NC_000013.11:g.98684567_98684568del, NC_000013.11:g.98684568del, NC_000013.11:g.98684568dup, NC_000013.11:g.98684567_98684568dup, NC_000013.11:g.98684566_98684568dup, NC_000013.11:g.98684565_98684568dup, NC_000013.11:g.98684564_98684568dup, NC_000013.11:g.98684563_98684568dup, NC_000013.11:g.98684562_98684568dup, NC_000013.11:g.98684561_98684568dup, NC_000013.11:g.98684560_98684568dup, NC_000013.11:g.98684559_98684568dup, NC_000013.11:g.98684558_98684568dup, NC_000013.11:g.98684557_98684568dup, NC_000013.11:g.98684556_98684568dup, NC_000013.11:g.98684555_98684568dup, NC_000013.11:g.98684553_98684568dup, NC_000013.11:g.98684552_98684568dup, NC_000013.11:g.98684551_98684568dup, NC_000013.11:g.98684550_98684568dup, NC_000013.11:g.98684549_98684568dup, NC_000013.11:g.98684547_98684568dup, NC_000013.11:g.98684546_98684568dup, NC_000013.11:g.98684568_98684569insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.98684568_98684569insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.98684568_98684569insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.98684568_98684569insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.98684568_98684569insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.98684568_98684569insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.98684546_98684568A[23]CAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000013.10:g.99336805_99336822del, NC_000013.10:g.99336810_99336822del, NC_000013.10:g.99336811_99336822del, NC_000013.10:g.99336812_99336822del, NC_000013.10:g.99336813_99336822del, NC_000013.10:g.99336814_99336822del, NC_000013.10:g.99336816_99336822del, NC_000013.10:g.99336817_99336822del, NC_000013.10:g.99336818_99336822del, NC_000013.10:g.99336819_99336822del, NC_000013.10:g.99336820_99336822del, NC_000013.10:g.99336821_99336822del, NC_000013.10:g.99336822del, NC_000013.10:g.99336822dup, NC_000013.10:g.99336821_99336822dup, NC_000013.10:g.99336820_99336822dup, NC_000013.10:g.99336819_99336822dup, NC_000013.10:g.99336818_99336822dup, NC_000013.10:g.99336817_99336822dup, NC_000013.10:g.99336816_99336822dup, NC_000013.10:g.99336815_99336822dup, NC_000013.10:g.99336814_99336822dup, NC_000013.10:g.99336813_99336822dup, NC_000013.10:g.99336812_99336822dup, NC_000013.10:g.99336811_99336822dup, NC_000013.10:g.99336810_99336822dup, NC_000013.10:g.99336809_99336822dup, NC_000013.10:g.99336807_99336822dup, NC_000013.10:g.99336806_99336822dup, NC_000013.10:g.99336805_99336822dup, NC_000013.10:g.99336804_99336822dup, NC_000013.10:g.99336803_99336822dup, NC_000013.10:g.99336801_99336822dup, NC_000013.10:g.99336800_99336822dup, NC_000013.10:g.99336822_99336823insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99336822_99336823insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99336822_99336823insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99336822_99336823insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99336822_99336823insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99336822_99336823insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99336800_99336822A[23]CAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_017032.1:g.73113_73130del, NG_017032.1:g.73118_73130del, NG_017032.1:g.73119_73130del, NG_017032.1:g.73120_73130del, NG_017032.1:g.73121_73130del, NG_017032.1:g.73122_73130del, NG_017032.1:g.73124_73130del, NG_017032.1:g.73125_73130del, NG_017032.1:g.73126_73130del, NG_017032.1:g.73127_73130del, NG_017032.1:g.73128_73130del, NG_017032.1:g.73129_73130del, NG_017032.1:g.73130del, NG_017032.1:g.73130dup, NG_017032.1:g.73129_73130dup, NG_017032.1:g.73128_73130dup, NG_017032.1:g.73127_73130dup, NG_017032.1:g.73126_73130dup, NG_017032.1:g.73125_73130dup, NG_017032.1:g.73124_73130dup, NG_017032.1:g.73123_73130dup, NG_017032.1:g.73122_73130dup, NG_017032.1:g.73121_73130dup, NG_017032.1:g.73120_73130dup, NG_017032.1:g.73119_73130dup, NG_017032.1:g.73118_73130dup, NG_017032.1:g.73117_73130dup, NG_017032.1:g.73115_73130dup, NG_017032.1:g.73114_73130dup, NG_017032.1:g.73113_73130dup, NG_017032.1:g.73112_73130dup, NG_017032.1:g.73111_73130dup, NG_017032.1:g.73109_73130dup, NG_017032.1:g.73108_73130dup, NG_017032.1:g.73130_73131insTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.73130_73131insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.73130_73131insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.73130_73131insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.73130_73131insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.73130_73131insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.73108_73130T[25]GTTTTTTTTTTTTTTTTTTTTTTT[1], NM_005073.4:c.*161_*178del, NM_005073.4:c.*166_*178del, NM_005073.4:c.*167_*178del, NM_005073.4:c.*168_*178del, NM_005073.4:c.*169_*178del, NM_005073.4:c.*170_*178del, NM_005073.4:c.*172_*178del, NM_005073.4:c.*173_*178del, NM_005073.4:c.*174_*178del, NM_005073.4:c.*175_*178del, NM_005073.4:c.*176_*178del, NM_005073.4:c.*177_*178del, NM_005073.4:c.*178del, NM_005073.4:c.*178dup, NM_005073.4:c.*177_*178dup, NM_005073.4:c.*176_*178dup, NM_005073.4:c.*175_*178dup, NM_005073.4:c.*174_*178dup, NM_005073.4:c.*173_*178dup, NM_005073.4:c.*172_*178dup, NM_005073.4:c.*171_*178dup, NM_005073.4:c.*170_*178dup, NM_005073.4:c.*169_*178dup, NM_005073.4:c.*168_*178dup, NM_005073.4:c.*167_*178dup, NM_005073.4:c.*166_*178dup, NM_005073.4:c.*165_*178dup, NM_005073.4:c.*163_*178dup, NM_005073.4:c.*162_*178dup, NM_005073.4:c.*161_*178dup, NM_005073.4:c.*160_*178dup, NM_005073.4:c.*159_*178dup, NM_005073.4:c.*157_*178dup, NM_005073.4:c.*156_*178dup, NM_005073.4:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.4:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.4:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.4:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.4:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.4:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.4:c.*156_*178T[25]GTTTTTTTTTTTTTTTTTTTTTTT[1], NM_005073.3:c.*161_*178del, NM_005073.3:c.*166_*178del, NM_005073.3:c.*167_*178del, NM_005073.3:c.*168_*178del, NM_005073.3:c.*169_*178del, NM_005073.3:c.*170_*178del, NM_005073.3:c.*172_*178del, NM_005073.3:c.*173_*178del, NM_005073.3:c.*174_*178del, NM_005073.3:c.*175_*178del, NM_005073.3:c.*176_*178del, NM_005073.3:c.*177_*178del, NM_005073.3:c.*178del, NM_005073.3:c.*178dup, NM_005073.3:c.*177_*178dup, NM_005073.3:c.*176_*178dup, NM_005073.3:c.*175_*178dup, NM_005073.3:c.*174_*178dup, NM_005073.3:c.*173_*178dup, NM_005073.3:c.*172_*178dup, NM_005073.3:c.*171_*178dup, NM_005073.3:c.*170_*178dup, NM_005073.3:c.*169_*178dup, NM_005073.3:c.*168_*178dup, NM_005073.3:c.*167_*178dup, NM_005073.3:c.*166_*178dup, NM_005073.3:c.*165_*178dup, NM_005073.3:c.*163_*178dup, NM_005073.3:c.*162_*178dup, NM_005073.3:c.*161_*178dup, NM_005073.3:c.*160_*178dup, NM_005073.3:c.*159_*178dup, NM_005073.3:c.*157_*178dup, NM_005073.3:c.*156_*178dup, NM_005073.3:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.3:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.3:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.3:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.3:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.3:c.*178_*179insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_005073.3:c.*156_*178T[25]GTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14915772442.

rs1491577244 has merged into rs61087152 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:98708980 (GRCh38)
13:99361234 (GRCh37)
Canonical SPDI:: NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98708967:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.3902/1954 (1000Genomes)
HGVS:: NC_000013.11:g.98708980_98708985del, NC_000013.11:g.98708982_98708985del, NC_000013.11:g.98708983_98708985del, NC_000013.11:g.98708984_98708985del, NC_000013.11:g.98708985del, NC_000013.11:g.98708985dup, NC_000013.11:g.98708984_98708985dup, NC_000013.11:g.98708983_98708985dup, NC_000013.11:g.98708982_98708985dup, NC_000013.11:g.98708981_98708985dup, NC_000013.11:g.98708979_98708985dup, NC_000013.10:g.99361234_99361239del, NC_000013.10:g.99361236_99361239del, NC_000013.10:g.99361237_99361239del, NC_000013.10:g.99361238_99361239del, NC_000013.10:g.99361239del, NC_000013.10:g.99361239dup, NC_000013.10:g.99361238_99361239dup, NC_000013.10:g.99361237_99361239dup, NC_000013.10:g.99361236_99361239dup, NC_000013.10:g.99361235_99361239dup, NC_000013.10:g.99361233_99361239dup, NG_017032.1:g.48703_48708del, NG_017032.1:g.48705_48708del, NG_017032.1:g.48706_48708del, NG_017032.1:g.48707_48708del, NG_017032.1:g.48708del, NG_017032.1:g.48708dup, NG_017032.1:g.48707_48708dup, NG_017032.1:g.48706_48708dup, NG_017032.1:g.48705_48708dup, NG_017032.1:g.48704_48708dup, NG_017032.1:g.48702_48708dup

Select item 14915700553.

rs1491570055 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 13:98684545 (GRCh38)
13:99336799 (GRCh37)
Canonical SPDI:: NC_000013.11:98684544:CA:
Gene:: SLC15A1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: -=0.00236/28 (ALFA)
-=0.00148/41 (TOMMO)
HGVS:: NC_000013.11:g.98684545_98684546del, NC_000013.10:g.99336799_99336800del, NG_017032.1:g.73130_73131del, NM_005073.4:c.*178_*179del, NM_005073.3:c.*178_*179del

Select item 14915305554.

rs1491530555 has merged into rs771426478 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:98703552 (GRCh38)
13:99355806 (GRCh37)
Canonical SPDI:: NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98703539:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTTTTT=0./0 (GENOME_DK)
HGVS:: NC_000013.11:g.98703552_98703574del, NC_000013.11:g.98703553_98703574del, NC_000013.11:g.98703554_98703574del, NC_000013.11:g.98703555_98703574del, NC_000013.11:g.98703556_98703574del, NC_000013.11:g.98703557_98703574del, NC_000013.11:g.98703558_98703574del, NC_000013.11:g.98703559_98703574del, NC_000013.11:g.98703560_98703574del, NC_000013.11:g.98703561_98703574del, NC_000013.11:g.98703562_98703574del, NC_000013.11:g.98703563_98703574del, NC_000013.11:g.98703564_98703574del, NC_000013.11:g.98703565_98703574del, NC_000013.11:g.98703566_98703574del, NC_000013.11:g.98703567_98703574del, NC_000013.11:g.98703568_98703574del, NC_000013.11:g.98703569_98703574del, NC_000013.11:g.98703570_98703574del, NC_000013.11:g.98703571_98703574del, NC_000013.11:g.98703572_98703574del, NC_000013.11:g.98703573_98703574del, NC_000013.11:g.98703574del, NC_000013.11:g.98703574dup, NC_000013.11:g.98703573_98703574dup, NC_000013.11:g.98703572_98703574dup, NC_000013.11:g.98703571_98703574dup, NC_000013.11:g.98703570_98703574dup, NC_000013.11:g.98703569_98703574dup, NC_000013.11:g.98703568_98703574dup, NC_000013.11:g.98703567_98703574dup, NC_000013.11:g.98703566_98703574dup, NC_000013.11:g.98703565_98703574dup, NC_000013.11:g.98703564_98703574dup, NC_000013.11:g.98703563_98703574dup, NC_000013.11:g.98703561_98703574dup, NC_000013.11:g.98703559_98703574dup, NC_000013.11:g.98703552_98703574dup, NC_000013.11:g.98703550_98703574dup, NC_000013.11:g.98703546_98703574dup, NC_000013.11:g.98703574_98703575insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000013.10:g.99355806_99355828del, NC_000013.10:g.99355807_99355828del, NC_000013.10:g.99355808_99355828del, NC_000013.10:g.99355809_99355828del, NC_000013.10:g.99355810_99355828del, NC_000013.10:g.99355811_99355828del, NC_000013.10:g.99355812_99355828del, NC_000013.10:g.99355813_99355828del, NC_000013.10:g.99355814_99355828del, NC_000013.10:g.99355815_99355828del, NC_000013.10:g.99355816_99355828del, NC_000013.10:g.99355817_99355828del, NC_000013.10:g.99355818_99355828del, NC_000013.10:g.99355819_99355828del, NC_000013.10:g.99355820_99355828del, NC_000013.10:g.99355821_99355828del, NC_000013.10:g.99355822_99355828del, NC_000013.10:g.99355823_99355828del, NC_000013.10:g.99355824_99355828del, NC_000013.10:g.99355825_99355828del, NC_000013.10:g.99355826_99355828del, NC_000013.10:g.99355827_99355828del, NC_000013.10:g.99355828del, NC_000013.10:g.99355828dup, NC_000013.10:g.99355827_99355828dup, NC_000013.10:g.99355826_99355828dup, NC_000013.10:g.99355825_99355828dup, NC_000013.10:g.99355824_99355828dup, NC_000013.10:g.99355823_99355828dup, NC_000013.10:g.99355822_99355828dup, NC_000013.10:g.99355821_99355828dup, NC_000013.10:g.99355820_99355828dup, NC_000013.10:g.99355819_99355828dup, NC_000013.10:g.99355818_99355828dup, NC_000013.10:g.99355817_99355828dup, NC_000013.10:g.99355815_99355828dup, NC_000013.10:g.99355813_99355828dup, NC_000013.10:g.99355806_99355828dup, NC_000013.10:g.99355804_99355828dup, NC_000013.10:g.99355800_99355828dup, NC_000013.10:g.99355828_99355829insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.54114_54136del, NG_017032.1:g.54115_54136del, NG_017032.1:g.54116_54136del, NG_017032.1:g.54117_54136del, NG_017032.1:g.54118_54136del, NG_017032.1:g.54119_54136del, NG_017032.1:g.54120_54136del, NG_017032.1:g.54121_54136del, NG_017032.1:g.54122_54136del, NG_017032.1:g.54123_54136del, NG_017032.1:g.54124_54136del, NG_017032.1:g.54125_54136del, NG_017032.1:g.54126_54136del, NG_017032.1:g.54127_54136del, NG_017032.1:g.54128_54136del, NG_017032.1:g.54129_54136del, NG_017032.1:g.54130_54136del, NG_017032.1:g.54131_54136del, NG_017032.1:g.54132_54136del, NG_017032.1:g.54133_54136del, NG_017032.1:g.54134_54136del, NG_017032.1:g.54135_54136del, NG_017032.1:g.54136del, NG_017032.1:g.54136dup, NG_017032.1:g.54135_54136dup, NG_017032.1:g.54134_54136dup, NG_017032.1:g.54133_54136dup, NG_017032.1:g.54132_54136dup, NG_017032.1:g.54131_54136dup, NG_017032.1:g.54130_54136dup, NG_017032.1:g.54129_54136dup, NG_017032.1:g.54128_54136dup, NG_017032.1:g.54127_54136dup, NG_017032.1:g.54126_54136dup, NG_017032.1:g.54125_54136dup, NG_017032.1:g.54123_54136dup, NG_017032.1:g.54121_54136dup, NG_017032.1:g.54114_54136dup, NG_017032.1:g.54112_54136dup, NG_017032.1:g.54108_54136dup, NG_017032.1:g.54136_54137insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14915191415.

rs1491519141 has merged into rs11309992 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:98686957 (GRCh38)
13:99339211 (GRCh37)
Canonical SPDI:: NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000013.11:98686949:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.98686957_98686965del, NC_000013.11:g.98686961_98686965del, NC_000013.11:g.98686962_98686965del, NC_000013.11:g.98686963_98686965del, NC_000013.11:g.98686964_98686965del, NC_000013.11:g.98686965del, NC_000013.11:g.98686965dup, NC_000013.11:g.98686964_98686965dup, NC_000013.11:g.98686963_98686965dup, NC_000013.11:g.98686962_98686965dup, NC_000013.11:g.98686958_98686965dup, NC_000013.10:g.99339211_99339219del, NC_000013.10:g.99339215_99339219del, NC_000013.10:g.99339216_99339219del, NC_000013.10:g.99339217_99339219del, NC_000013.10:g.99339218_99339219del, NC_000013.10:g.99339219del, NC_000013.10:g.99339219dup, NC_000013.10:g.99339218_99339219dup, NC_000013.10:g.99339217_99339219dup, NC_000013.10:g.99339216_99339219dup, NC_000013.10:g.99339212_99339219dup, NG_017032.1:g.70718_70726del, NG_017032.1:g.70722_70726del, NG_017032.1:g.70723_70726del, NG_017032.1:g.70724_70726del, NG_017032.1:g.70725_70726del, NG_017032.1:g.70726del, NG_017032.1:g.70726dup, NG_017032.1:g.70725_70726dup, NG_017032.1:g.70724_70726dup, NG_017032.1:g.70723_70726dup, NG_017032.1:g.70719_70726dup

Select item 14915152216.

rs1491515221 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 13:98753202 (GRCh38)
13:99405456 (GRCh37)
Canonical SPDI:: NC_000013.11:98753201:AT:
Gene:: SLC15A1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000356/5 (ALFA)
-=0./0 (TWINSUK)
-=0.000259/1 (ALSPAC)
-=0.00038/53 (GnomAD)
-=0.000442/117 (TOPMED)
-=0.001562/10 (1000Genomes)
HGVS:: NC_000013.11:g.98753202_98753203del, NC_000013.10:g.99405456_99405457del, NG_017032.1:g.4473_4474del

Select item 14914897407.

rs1491489740 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 13:98714059 (GRCh38)
13:99366313 (GRCh37)
Canonical SPDI:: NC_000013.11:98714058:GA:
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00782/29 (TWINSUK)
-=0.01271/49 (ALSPAC)
HGVS:: NC_000013.11:g.98714059_98714060del, NC_000013.10:g.99366313_99366314del, NG_017032.1:g.43616_43617del

Select item 14914834708.

rs1491483470 has merged into rs4646225 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:98710819 (GRCh38)
13:99363073 (GRCh37)
Canonical SPDI:: NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98710808:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.175/7 (GENOME_DK)
HGVS:: NC_000013.11:g.98710819_98710832del, NC_000013.11:g.98710820_98710832del, NC_000013.11:g.98710821_98710832del, NC_000013.11:g.98710822_98710832del, NC_000013.11:g.98710823_98710832del, NC_000013.11:g.98710824_98710832del, NC_000013.11:g.98710825_98710832del, NC_000013.11:g.98710826_98710832del, NC_000013.11:g.98710827_98710832del, NC_000013.11:g.98710828_98710832del, NC_000013.11:g.98710829_98710832del, NC_000013.11:g.98710830_98710832del, NC_000013.11:g.98710831_98710832del, NC_000013.11:g.98710832del, NC_000013.11:g.98710832dup, NC_000013.11:g.98710831_98710832dup, NC_000013.11:g.98710830_98710832dup, NC_000013.11:g.98710829_98710832dup, NC_000013.11:g.98710828_98710832dup, NC_000013.11:g.98710827_98710832dup, NC_000013.11:g.98710826_98710832dup, NC_000013.11:g.98710825_98710832dup, NC_000013.11:g.98710824_98710832dup, NC_000013.11:g.98710810_98710832dup, NC_000013.11:g.98710832_98710833insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99363073_99363086del, NC_000013.10:g.99363074_99363086del, NC_000013.10:g.99363075_99363086del, NC_000013.10:g.99363076_99363086del, NC_000013.10:g.99363077_99363086del, NC_000013.10:g.99363078_99363086del, NC_000013.10:g.99363079_99363086del, NC_000013.10:g.99363080_99363086del, NC_000013.10:g.99363081_99363086del, NC_000013.10:g.99363082_99363086del, NC_000013.10:g.99363083_99363086del, NC_000013.10:g.99363084_99363086del, NC_000013.10:g.99363085_99363086del, NC_000013.10:g.99363086del, NC_000013.10:g.99363086dup, NC_000013.10:g.99363085_99363086dup, NC_000013.10:g.99363084_99363086dup, NC_000013.10:g.99363083_99363086dup, NC_000013.10:g.99363082_99363086dup, NC_000013.10:g.99363081_99363086dup, NC_000013.10:g.99363080_99363086dup, NC_000013.10:g.99363079_99363086dup, NC_000013.10:g.99363078_99363086dup, NC_000013.10:g.99363064_99363086dup, NC_000013.10:g.99363086_99363087insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_017032.1:g.46854_46867del, NG_017032.1:g.46855_46867del, NG_017032.1:g.46856_46867del, NG_017032.1:g.46857_46867del, NG_017032.1:g.46858_46867del, NG_017032.1:g.46859_46867del, NG_017032.1:g.46860_46867del, NG_017032.1:g.46861_46867del, NG_017032.1:g.46862_46867del, NG_017032.1:g.46863_46867del, NG_017032.1:g.46864_46867del, NG_017032.1:g.46865_46867del, NG_017032.1:g.46866_46867del, NG_017032.1:g.46867del, NG_017032.1:g.46867dup, NG_017032.1:g.46866_46867dup, NG_017032.1:g.46865_46867dup, NG_017032.1:g.46864_46867dup, NG_017032.1:g.46863_46867dup, NG_017032.1:g.46862_46867dup, NG_017032.1:g.46861_46867dup, NG_017032.1:g.46860_46867dup, NG_017032.1:g.46859_46867dup, NG_017032.1:g.46845_46867dup, NG_017032.1:g.46867_46868insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14914514829.

rs1491451482 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGA>-,GA,GAGAGA [Show Flanks]
Chromosome:: 13:98753084 (GRCh38)
13:99405338 (GRCh37)
Canonical SPDI:: NC_000013.11:98753079:GAGAGAGA:GAGA,NC_000013.11:98753079:GAGAGAGA:GAGAGA,NC_000013.11:98753079:GAGAGAGA:GAGAGAGAGA
Gene:: SLC15A1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
GA=0.000008/1 (GnomAD)
-=0.000546/1 (Korea1K)
HGVS:: NC_000013.11:g.98753080GA[2], NC_000013.11:g.98753080GA[3], NC_000013.11:g.98753080GA[5], NC_000013.10:g.99405334GA[2], NC_000013.10:g.99405334GA[3], NC_000013.10:g.99405334GA[5], NG_017032.1:g.4589TC[2], NG_017032.1:g.4589TC[3], NG_017032.1:g.4589TC[5]

Select item 149141898310.

rs1491418983 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 13:98702967 (GRCh38)
13:99355221 (GRCh37)
Canonical SPDI:: NC_000013.11:98702966:CA:
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00363/43 (ALFA)
HGVS:: NC_000013.11:g.98702967_98702968del, NC_000013.10:g.99355221_99355222del, NG_017032.1:g.54708_54709del

Select item 149134602811.

rs1491346028 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAAATAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:98710809 (GRCh38)
13:99363064 (GRCh37)
Canonical SPDI:: NC_000013.11:98710809:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000013.11:g.98710810_98710832A[27]TAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000013.10:g.99363064_99363086A[27]TAAAAAAAAAAAAAAAAAAAAAAA[1], NG_017032.1:g.46844_46866T[23]ATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149131549312.

rs1491315493 has merged into rs528865683 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:98692149 (GRCh38)
13:99344403 (GRCh37)
Canonical SPDI:: NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:98692136:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTTTT=0.4421/2214 (1000Genomes)
HGVS:: NC_000013.11:g.98692149_98692171del, NC_000013.11:g.98692150_98692171del, NC_000013.11:g.98692151_98692171del, NC_000013.11:g.98692152_98692171del, NC_000013.11:g.98692153_98692171del, NC_000013.11:g.98692154_98692171del, NC_000013.11:g.98692155_98692171del, NC_000013.11:g.98692156_98692171del, NC_000013.11:g.98692157_98692171del, NC_000013.11:g.98692158_98692171del, NC_000013.11:g.98692159_98692171del, NC_000013.11:g.98692160_98692171del, NC_000013.11:g.98692161_98692171del, NC_000013.11:g.98692162_98692171del, NC_000013.11:g.98692163_98692171del, NC_000013.11:g.98692164_98692171del, NC_000013.11:g.98692165_98692171del, NC_000013.11:g.98692166_98692171del, NC_000013.11:g.98692167_98692171del, NC_000013.11:g.98692168_98692171del, NC_000013.11:g.98692169_98692171del, NC_000013.11:g.98692170_98692171del, NC_000013.11:g.98692171del, NC_000013.11:g.98692171dup, NC_000013.11:g.98692170_98692171dup, NC_000013.11:g.98692169_98692171dup, NC_000013.11:g.98692168_98692171dup, NC_000013.11:g.98692167_98692171dup, NC_000013.11:g.98692166_98692171dup, NC_000013.11:g.98692165_98692171dup, NC_000013.11:g.98692164_98692171dup, NC_000013.11:g.98692163_98692171dup, NC_000013.11:g.98692162_98692171dup, NC_000013.11:g.98692161_98692171dup, NC_000013.11:g.98692160_98692171dup, NC_000013.11:g.98692158_98692171dup, NC_000013.10:g.99344403_99344425del, NC_000013.10:g.99344404_99344425del, NC_000013.10:g.99344405_99344425del, NC_000013.10:g.99344406_99344425del, NC_000013.10:g.99344407_99344425del, NC_000013.10:g.99344408_99344425del, NC_000013.10:g.99344409_99344425del, NC_000013.10:g.99344410_99344425del, NC_000013.10:g.99344411_99344425del, NC_000013.10:g.99344412_99344425del, NC_000013.10:g.99344413_99344425del, NC_000013.10:g.99344414_99344425del, NC_000013.10:g.99344415_99344425del, NC_000013.10:g.99344416_99344425del, NC_000013.10:g.99344417_99344425del, NC_000013.10:g.99344418_99344425del, NC_000013.10:g.99344419_99344425del, NC_000013.10:g.99344420_99344425del, NC_000013.10:g.99344421_99344425del, NC_000013.10:g.99344422_99344425del, NC_000013.10:g.99344423_99344425del, NC_000013.10:g.99344424_99344425del, NC_000013.10:g.99344425del, NC_000013.10:g.99344425dup, NC_000013.10:g.99344424_99344425dup, NC_000013.10:g.99344423_99344425dup, NC_000013.10:g.99344422_99344425dup, NC_000013.10:g.99344421_99344425dup, NC_000013.10:g.99344420_99344425dup, NC_000013.10:g.99344419_99344425dup, NC_000013.10:g.99344418_99344425dup, NC_000013.10:g.99344417_99344425dup, NC_000013.10:g.99344416_99344425dup, NC_000013.10:g.99344415_99344425dup, NC_000013.10:g.99344414_99344425dup, NC_000013.10:g.99344412_99344425dup, NG_017032.1:g.65517_65539del, NG_017032.1:g.65518_65539del, NG_017032.1:g.65519_65539del, NG_017032.1:g.65520_65539del, NG_017032.1:g.65521_65539del, NG_017032.1:g.65522_65539del, NG_017032.1:g.65523_65539del, NG_017032.1:g.65524_65539del, NG_017032.1:g.65525_65539del, NG_017032.1:g.65526_65539del, NG_017032.1:g.65527_65539del, NG_017032.1:g.65528_65539del, NG_017032.1:g.65529_65539del, NG_017032.1:g.65530_65539del, NG_017032.1:g.65531_65539del, NG_017032.1:g.65532_65539del, NG_017032.1:g.65533_65539del, NG_017032.1:g.65534_65539del, NG_017032.1:g.65535_65539del, NG_017032.1:g.65536_65539del, NG_017032.1:g.65537_65539del, NG_017032.1:g.65538_65539del, NG_017032.1:g.65539del, NG_017032.1:g.65539dup, NG_017032.1:g.65538_65539dup, NG_017032.1:g.65537_65539dup, NG_017032.1:g.65536_65539dup, NG_017032.1:g.65535_65539dup, NG_017032.1:g.65534_65539dup, NG_017032.1:g.65533_65539dup, NG_017032.1:g.65532_65539dup, NG_017032.1:g.65531_65539dup, NG_017032.1:g.65530_65539dup, NG_017032.1:g.65529_65539dup, NG_017032.1:g.65528_65539dup, NG_017032.1:g.65526_65539dup

Select item 149130944713.

rs1491309447 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 13:98697636 (GRCh38)
13:99349890 (GRCh37)
Canonical SPDI:: NC_000013.11:98697635:TA:
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.001286/21 (ALFA)
-=0.001307/182 (GnomAD)
HGVS:: NC_000013.11:g.98697636_98697637del, NC_000013.10:g.99349890_99349891del, NG_017032.1:g.60039_60040del

Select item 149127240314.

rs1491272403 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->AT
Chromosome:: no mapping
Canonical SPDI:

Select item 149126471615.

rs1491264716 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 13:98695020 (GRCh38)
13:99347274 (GRCh37)
Canonical SPDI:: NC_000013.11:98695019:CA:
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00067/8 (ALFA)
HGVS:: NC_000013.11:g.98695020_98695021del, NC_000013.10:g.99347274_99347275del, NG_017032.1:g.62655_62656del

Select item 149125183116.

rs1491251831 has merged into rs1170231960 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:98695037 (GRCh38)
13:99347291 (GRCh37)
Canonical SPDI:: NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98695020:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000013.11:g.98695037_98695041del, NC_000013.11:g.98695038_98695041del, NC_000013.11:g.98695039_98695041del, NC_000013.11:g.98695040_98695041del, NC_000013.11:g.98695041del, NC_000013.11:g.98695041dup, NC_000013.11:g.98695040_98695041dup, NC_000013.11:g.98695039_98695041dup, NC_000013.11:g.98695038_98695041dup, NC_000013.11:g.98695037_98695041dup, NC_000013.11:g.98695036_98695041dup, NC_000013.11:g.98695035_98695041dup, NC_000013.11:g.98695034_98695041dup, NC_000013.11:g.98695033_98695041dup, NC_000013.11:g.98695031_98695041dup, NC_000013.10:g.99347291_99347295del, NC_000013.10:g.99347292_99347295del, NC_000013.10:g.99347293_99347295del, NC_000013.10:g.99347294_99347295del, NC_000013.10:g.99347295del, NC_000013.10:g.99347295dup, NC_000013.10:g.99347294_99347295dup, NC_000013.10:g.99347293_99347295dup, NC_000013.10:g.99347292_99347295dup, NC_000013.10:g.99347291_99347295dup, NC_000013.10:g.99347290_99347295dup, NC_000013.10:g.99347289_99347295dup, NC_000013.10:g.99347288_99347295dup, NC_000013.10:g.99347287_99347295dup, NC_000013.10:g.99347285_99347295dup, NG_017032.1:g.62651_62655del, NG_017032.1:g.62652_62655del, NG_017032.1:g.62653_62655del, NG_017032.1:g.62654_62655del, NG_017032.1:g.62655del, NG_017032.1:g.62655dup, NG_017032.1:g.62654_62655dup, NG_017032.1:g.62653_62655dup, NG_017032.1:g.62652_62655dup, NG_017032.1:g.62651_62655dup, NG_017032.1:g.62650_62655dup, NG_017032.1:g.62649_62655dup, NG_017032.1:g.62648_62655dup, NG_017032.1:g.62647_62655dup, NG_017032.1:g.62645_62655dup

Select item 149123662217.

rs1491236622 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 13:98744748 (GRCh38)
13:99397002 (GRCh37)
Canonical SPDI:: NC_000013.11:98744747:CA:
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00481/57 (ALFA)
HGVS:: NC_000013.11:g.98744748_98744749del, NC_000013.10:g.99397002_99397003del, NG_017032.1:g.12927_12928del

Select item 149123573618.

rs1491235736 has merged into rs58621986 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:98705906 (GRCh38)
13:99358160 (GRCh37)
Canonical SPDI:: NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98705893:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
AA=0.4261/2134 (1000Genomes)
HGVS:: NC_000013.11:g.98705906_98705912del, NC_000013.11:g.98705908_98705912del, NC_000013.11:g.98705909_98705912del, NC_000013.11:g.98705910_98705912del, NC_000013.11:g.98705911_98705912del, NC_000013.11:g.98705912del, NC_000013.11:g.98705912dup, NC_000013.11:g.98705911_98705912dup, NC_000013.11:g.98705910_98705912dup, NC_000013.11:g.98705909_98705912dup, NC_000013.11:g.98705908_98705912dup, NC_000013.11:g.98705905_98705912dup, NC_000013.10:g.99358160_99358166del, NC_000013.10:g.99358162_99358166del, NC_000013.10:g.99358163_99358166del, NC_000013.10:g.99358164_99358166del, NC_000013.10:g.99358165_99358166del, NC_000013.10:g.99358166del, NC_000013.10:g.99358166dup, NC_000013.10:g.99358165_99358166dup, NC_000013.10:g.99358164_99358166dup, NC_000013.10:g.99358163_99358166dup, NC_000013.10:g.99358162_99358166dup, NC_000013.10:g.99358159_99358166dup, NG_017032.1:g.51776_51782del, NG_017032.1:g.51778_51782del, NG_017032.1:g.51779_51782del, NG_017032.1:g.51780_51782del, NG_017032.1:g.51781_51782del, NG_017032.1:g.51782del, NG_017032.1:g.51782dup, NG_017032.1:g.51781_51782dup, NG_017032.1:g.51780_51782dup, NG_017032.1:g.51779_51782dup, NG_017032.1:g.51778_51782dup, NG_017032.1:g.51775_51782dup

Select item 149122935219.

rs1491229352 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACAG [Show Flanks]
Chromosome:: 13:98747782 (GRCh38)
13:99400037 (GRCh37)
Canonical SPDI:: NC_000013.11:98747782:AGACAG:AGACAGACAG
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AGACAGACAG=0./0 (ALFA)
AGAC=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.98747785_98747788dup, NC_000013.10:g.99400039_99400042dup, NG_017032.1:g.9890_9893dup

Select item 149121950120.

rs1491219501 has merged into rs5806073 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:98744758 (GRCh38)
13:99397012 (GRCh37)
Canonical SPDI:: NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:98744748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SLC15A1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.0322/124 (ALSPAC)
HGVS:: NC_000013.11:g.98744758_98744772del, NC_000013.11:g.98744759_98744772del, NC_000013.11:g.98744760_98744772del, NC_000013.11:g.98744761_98744772del, NC_000013.11:g.98744762_98744772del, NC_000013.11:g.98744763_98744772del, NC_000013.11:g.98744764_98744772del, NC_000013.11:g.98744765_98744772del, NC_000013.11:g.98744766_98744772del, NC_000013.11:g.98744767_98744772del, NC_000013.11:g.98744768_98744772del, NC_000013.11:g.98744769_98744772del, NC_000013.11:g.98744770_98744772del, NC_000013.11:g.98744771_98744772del, NC_000013.11:g.98744772del, NC_000013.11:g.98744772dup, NC_000013.11:g.98744771_98744772dup, NC_000013.11:g.98744770_98744772dup, NC_000013.11:g.98744769_98744772dup, NC_000013.11:g.98744768_98744772dup, NC_000013.11:g.98744767_98744772dup, NC_000013.11:g.98744766_98744772dup, NC_000013.11:g.98744765_98744772dup, NC_000013.11:g.98744758_98744772dup, NC_000013.11:g.98744756_98744772dup, NC_000013.11:g.98744751_98744772dup, NC_000013.11:g.98744772_98744773insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.98744772_98744773insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99397012_99397026del, NC_000013.10:g.99397013_99397026del, NC_000013.10:g.99397014_99397026del, NC_000013.10:g.99397015_99397026del, NC_000013.10:g.99397016_99397026del, NC_000013.10:g.99397017_99397026del, NC_000013.10:g.99397018_99397026del, NC_000013.10:g.99397019_99397026del, NC_000013.10:g.99397020_99397026del, NC_000013.10:g.99397021_99397026del, NC_000013.10:g.99397022_99397026del, NC_000013.10:g.99397023_99397026del, NC_000013.10:g.99397024_99397026del, NC_000013.10:g.99397025_99397026del, NC_000013.10:g.99397026del, NC_000013.10:g.99397026dup, NC_000013.10:g.99397025_99397026dup, NC_000013.10:g.99397024_99397026dup, NC_000013.10:g.99397023_99397026dup, NC_000013.10:g.99397022_99397026dup, NC_000013.10:g.99397021_99397026dup, NC_000013.10:g.99397020_99397026dup, NC_000013.10:g.99397019_99397026dup, NC_000013.10:g.99397012_99397026dup, NC_000013.10:g.99397010_99397026dup, NC_000013.10:g.99397005_99397026dup, NC_000013.10:g.99397026_99397027insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.99397026_99397027insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_017032.1:g.12913_12927del, NG_017032.1:g.12914_12927del, NG_017032.1:g.12915_12927del, NG_017032.1:g.12916_12927del, NG_017032.1:g.12917_12927del, NG_017032.1:g.12918_12927del, NG_017032.1:g.12919_12927del, NG_017032.1:g.12920_12927del, NG_017032.1:g.12921_12927del, NG_017032.1:g.12922_12927del, NG_017032.1:g.12923_12927del, NG_017032.1:g.12924_12927del, NG_017032.1:g.12925_12927del, NG_017032.1:g.12926_12927del, NG_017032.1:g.12927del, NG_017032.1:g.12927dup, NG_017032.1:g.12926_12927dup, NG_017032.1:g.12925_12927dup, NG_017032.1:g.12924_12927dup, NG_017032.1:g.12923_12927dup, NG_017032.1:g.12922_12927dup, NG_017032.1:g.12921_12927dup, NG_017032.1:g.12920_12927dup, NG_017032.1:g.12913_12927dup, NG_017032.1:g.12911_12927dup, NG_017032.1:g.12906_12927dup, NG_017032.1:g.12927_12928insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_017032.1:g.12927_12928insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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