SNP Links for Gene (Select 126282) - SNP

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Select item 14915844541.

rs1491584454 has merged into rs3070720 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:4638815 (GRCh38)
19:4638827 (GRCh37)
Canonical SPDI:: NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:4638805:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000019.10:g.4638815_4638822del, NC_000019.10:g.4638816_4638822del, NC_000019.10:g.4638817_4638822del, NC_000019.10:g.4638818_4638822del, NC_000019.10:g.4638819_4638822del, NC_000019.10:g.4638820_4638822del, NC_000019.10:g.4638821_4638822del, NC_000019.10:g.4638822del, NC_000019.10:g.4638822dup, NC_000019.10:g.4638821_4638822dup, NC_000019.10:g.4638820_4638822dup, NC_000019.10:g.4638819_4638822dup, NC_000019.10:g.4638818_4638822dup, NC_000019.10:g.4638817_4638822dup, NC_000019.10:g.4638815_4638822dup, NC_000019.10:g.4638814_4638822dup, NC_000019.10:g.4638809_4638822dup, NC_000019.10:g.4638807_4638822dup, NC_000019.10:g.4638806_4638822dup, NC_000019.10:g.4638822_4638823insTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.4638827_4638834del, NC_000019.9:g.4638828_4638834del, NC_000019.9:g.4638829_4638834del, NC_000019.9:g.4638830_4638834del, NC_000019.9:g.4638831_4638834del, NC_000019.9:g.4638832_4638834del, NC_000019.9:g.4638833_4638834del, NC_000019.9:g.4638834del, NC_000019.9:g.4638834dup, NC_000019.9:g.4638833_4638834dup, NC_000019.9:g.4638832_4638834dup, NC_000019.9:g.4638831_4638834dup, NC_000019.9:g.4638830_4638834dup, NC_000019.9:g.4638829_4638834dup, NC_000019.9:g.4638827_4638834dup, NC_000019.9:g.4638826_4638834dup, NC_000019.9:g.4638821_4638834dup, NC_000019.9:g.4638819_4638834dup, NC_000019.9:g.4638818_4638834dup, NC_000019.9:g.4638834_4638835insTTTTTTTTTTTTTTTTTTTT

Select item 14914646162.

rs1491464616 has merged into rs74173015 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:4653781 (GRCh38)
19:4653793 (GRCh37)
Canonical SPDI:: NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.4653781_4653797del, NC_000019.10:g.4653782_4653797del, NC_000019.10:g.4653783_4653797del, NC_000019.10:g.4653784_4653797del, NC_000019.10:g.4653785_4653797del, NC_000019.10:g.4653786_4653797del, NC_000019.10:g.4653787_4653797del, NC_000019.10:g.4653788_4653797del, NC_000019.10:g.4653789_4653797del, NC_000019.10:g.4653790_4653797del, NC_000019.10:g.4653791_4653797del, NC_000019.10:g.4653792_4653797del, NC_000019.10:g.4653793_4653797del, NC_000019.10:g.4653794_4653797del, NC_000019.10:g.4653795_4653797del, NC_000019.10:g.4653796_4653797del, NC_000019.10:g.4653797del, NC_000019.10:g.4653797dup, NC_000019.10:g.4653796_4653797dup, NC_000019.10:g.4653795_4653797dup, NC_000019.10:g.4653794_4653797dup, NC_000019.10:g.4653793_4653797dup, NC_000019.10:g.4653792_4653797dup, NC_000019.10:g.4653790_4653797dup, NC_000019.10:g.4653788_4653797dup, NC_000019.10:g.4653797_4653798insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.4653793_4653809del, NC_000019.9:g.4653794_4653809del, NC_000019.9:g.4653795_4653809del, NC_000019.9:g.4653796_4653809del, NC_000019.9:g.4653797_4653809del, NC_000019.9:g.4653798_4653809del, NC_000019.9:g.4653799_4653809del, NC_000019.9:g.4653800_4653809del, NC_000019.9:g.4653801_4653809del, NC_000019.9:g.4653802_4653809del, NC_000019.9:g.4653803_4653809del, NC_000019.9:g.4653804_4653809del, NC_000019.9:g.4653805_4653809del, NC_000019.9:g.4653806_4653809del, NC_000019.9:g.4653807_4653809del, NC_000019.9:g.4653808_4653809del, NC_000019.9:g.4653809del, NC_000019.9:g.4653809dup, NC_000019.9:g.4653808_4653809dup, NC_000019.9:g.4653807_4653809dup, NC_000019.9:g.4653806_4653809dup, NC_000019.9:g.4653805_4653809dup, NC_000019.9:g.4653804_4653809dup, NC_000019.9:g.4653802_4653809dup, NC_000019.9:g.4653800_4653809dup, NC_000019.9:g.4653809_4653810insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_005259487.4:c.*1351_*1367del, XM_005259487.4:c.*1352_*1367del, XM_005259487.4:c.*1353_*1367del, XM_005259487.4:c.*1354_*1367del, XM_005259487.4:c.*1355_*1367del, XM_005259487.4:c.*1356_*1367del, XM_005259487.4:c.*1357_*1367del, XM_005259487.4:c.*1358_*1367del, XM_005259487.4:c.*1359_*1367del, XM_005259487.4:c.*1360_*1367del, XM_005259487.4:c.*1361_*1367del, XM_005259487.4:c.*1362_*1367del, XM_005259487.4:c.*1363_*1367del, XM_005259487.4:c.*1364_*1367del, XM_005259487.4:c.*1365_*1367del, XM_005259487.4:c.*1366_*1367del, XM_005259487.4:c.*1367del, XM_005259487.4:c.*1367dup, XM_005259487.4:c.*1366_*1367dup, XM_005259487.4:c.*1365_*1367dup, XM_005259487.4:c.*1364_*1367dup, XM_005259487.4:c.*1363_*1367dup, XM_005259487.4:c.*1362_*1367dup, XM_005259487.4:c.*1360_*1367dup, XM_005259487.4:c.*1358_*1367dup, XM_005259487.4:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_005259487.3:c.*1351_*1367del, XM_005259487.3:c.*1352_*1367del, XM_005259487.3:c.*1353_*1367del, XM_005259487.3:c.*1354_*1367del, XM_005259487.3:c.*1355_*1367del, XM_005259487.3:c.*1356_*1367del, XM_005259487.3:c.*1357_*1367del, XM_005259487.3:c.*1358_*1367del, XM_005259487.3:c.*1359_*1367del, XM_005259487.3:c.*1360_*1367del, XM_005259487.3:c.*1361_*1367del, XM_005259487.3:c.*1362_*1367del, XM_005259487.3:c.*1363_*1367del, XM_005259487.3:c.*1364_*1367del, XM_005259487.3:c.*1365_*1367del, XM_005259487.3:c.*1366_*1367del, XM_005259487.3:c.*1367del, XM_005259487.3:c.*1367dup, XM_005259487.3:c.*1366_*1367dup, XM_005259487.3:c.*1365_*1367dup, XM_005259487.3:c.*1364_*1367dup, XM_005259487.3:c.*1363_*1367dup, XM_005259487.3:c.*1362_*1367dup, XM_005259487.3:c.*1360_*1367dup, XM_005259487.3:c.*1358_*1367dup, XM_005259487.3:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_152362.3:c.*1351_*1367del, NM_152362.3:c.*1352_*1367del, NM_152362.3:c.*1353_*1367del, NM_152362.3:c.*1354_*1367del, NM_152362.3:c.*1355_*1367del, NM_152362.3:c.*1356_*1367del, NM_152362.3:c.*1357_*1367del, NM_152362.3:c.*1358_*1367del, NM_152362.3:c.*1359_*1367del, NM_152362.3:c.*1360_*1367del, NM_152362.3:c.*1361_*1367del, NM_152362.3:c.*1362_*1367del, NM_152362.3:c.*1363_*1367del, NM_152362.3:c.*1364_*1367del, NM_152362.3:c.*1365_*1367del, NM_152362.3:c.*1366_*1367del, NM_152362.3:c.*1367del, NM_152362.3:c.*1367dup, NM_152362.3:c.*1366_*1367dup, NM_152362.3:c.*1365_*1367dup, NM_152362.3:c.*1364_*1367dup, NM_152362.3:c.*1363_*1367dup, NM_152362.3:c.*1362_*1367dup, NM_152362.3:c.*1360_*1367dup, NM_152362.3:c.*1358_*1367dup, NM_152362.3:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_152362.2:c.*1351_*1367del, NM_152362.2:c.*1352_*1367del, NM_152362.2:c.*1353_*1367del, NM_152362.2:c.*1354_*1367del, NM_152362.2:c.*1355_*1367del, NM_152362.2:c.*1356_*1367del, NM_152362.2:c.*1357_*1367del, NM_152362.2:c.*1358_*1367del, NM_152362.2:c.*1359_*1367del, NM_152362.2:c.*1360_*1367del, NM_152362.2:c.*1361_*1367del, NM_152362.2:c.*1362_*1367del, NM_152362.2:c.*1363_*1367del, NM_152362.2:c.*1364_*1367del, NM_152362.2:c.*1365_*1367del, NM_152362.2:c.*1366_*1367del, NM_152362.2:c.*1367del, NM_152362.2:c.*1367dup, NM_152362.2:c.*1366_*1367dup, NM_152362.2:c.*1365_*1367dup, NM_152362.2:c.*1364_*1367dup, NM_152362.2:c.*1363_*1367dup, NM_152362.2:c.*1362_*1367dup, NM_152362.2:c.*1360_*1367dup, NM_152362.2:c.*1358_*1367dup, NM_152362.2:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_011527680.3:c.*1351_*1367del, XM_011527680.3:c.*1352_*1367del, XM_011527680.3:c.*1353_*1367del, XM_011527680.3:c.*1354_*1367del, XM_011527680.3:c.*1355_*1367del, XM_011527680.3:c.*1356_*1367del, XM_011527680.3:c.*1357_*1367del, XM_011527680.3:c.*1358_*1367del, XM_011527680.3:c.*1359_*1367del, XM_011527680.3:c.*1360_*1367del, XM_011527680.3:c.*1361_*1367del, XM_011527680.3:c.*1362_*1367del, XM_011527680.3:c.*1363_*1367del, XM_011527680.3:c.*1364_*1367del, XM_011527680.3:c.*1365_*1367del, XM_011527680.3:c.*1366_*1367del, XM_011527680.3:c.*1367del, XM_011527680.3:c.*1367dup, XM_011527680.3:c.*1366_*1367dup, XM_011527680.3:c.*1365_*1367dup, XM_011527680.3:c.*1364_*1367dup, XM_011527680.3:c.*1363_*1367dup, XM_011527680.3:c.*1362_*1367dup, XM_011527680.3:c.*1360_*1367dup, XM_011527680.3:c.*1358_*1367dup, XM_011527680.3:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_011527680.2:c.*1351_*1367del, XM_011527680.2:c.*1352_*1367del, XM_011527680.2:c.*1353_*1367del, XM_011527680.2:c.*1354_*1367del, XM_011527680.2:c.*1355_*1367del, XM_011527680.2:c.*1356_*1367del, XM_011527680.2:c.*1357_*1367del, XM_011527680.2:c.*1358_*1367del, XM_011527680.2:c.*1359_*1367del, XM_011527680.2:c.*1360_*1367del, XM_011527680.2:c.*1361_*1367del, XM_011527680.2:c.*1362_*1367del, XM_011527680.2:c.*1363_*1367del, XM_011527680.2:c.*1364_*1367del, XM_011527680.2:c.*1365_*1367del, XM_011527680.2:c.*1366_*1367del, XM_011527680.2:c.*1367del, XM_011527680.2:c.*1367dup, XM_011527680.2:c.*1366_*1367dup, XM_011527680.2:c.*1365_*1367dup, XM_011527680.2:c.*1364_*1367dup, XM_011527680.2:c.*1363_*1367dup, XM_011527680.2:c.*1362_*1367dup, XM_011527680.2:c.*1360_*1367dup, XM_011527680.2:c.*1358_*1367dup, XM_011527680.2:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001167942.1:c.*1351_*1367del, NM_001167942.1:c.*1352_*1367del, NM_001167942.1:c.*1353_*1367del, NM_001167942.1:c.*1354_*1367del, NM_001167942.1:c.*1355_*1367del, NM_001167942.1:c.*1356_*1367del, NM_001167942.1:c.*1357_*1367del, NM_001167942.1:c.*1358_*1367del, NM_001167942.1:c.*1359_*1367del, NM_001167942.1:c.*1360_*1367del, NM_001167942.1:c.*1361_*1367del, NM_001167942.1:c.*1362_*1367del, NM_001167942.1:c.*1363_*1367del, NM_001167942.1:c.*1364_*1367del, NM_001167942.1:c.*1365_*1367del, NM_001167942.1:c.*1366_*1367del, NM_001167942.1:c.*1367del, NM_001167942.1:c.*1367dup, NM_001167942.1:c.*1366_*1367dup, NM_001167942.1:c.*1365_*1367dup, NM_001167942.1:c.*1364_*1367dup, NM_001167942.1:c.*1363_*1367dup, NM_001167942.1:c.*1362_*1367dup, NM_001167942.1:c.*1360_*1367dup, NM_001167942.1:c.*1358_*1367dup, NM_001167942.1:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14914094913.

rs1491409491 has merged into rs56182452 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:4642495 (GRCh38)
19:4642507 (GRCh37)
Canonical SPDI:: NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:4642482:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.4642495_4642498del, NC_000019.10:g.4642496_4642498del, NC_000019.10:g.4642497_4642498del, NC_000019.10:g.4642498del, NC_000019.10:g.4642498dup, NC_000019.10:g.4642497_4642498dup, NC_000019.10:g.4642496_4642498dup, NC_000019.10:g.4642490_4642498dup, NC_000019.9:g.4642507_4642510del, NC_000019.9:g.4642508_4642510del, NC_000019.9:g.4642509_4642510del, NC_000019.9:g.4642510del, NC_000019.9:g.4642510dup, NC_000019.9:g.4642509_4642510dup, NC_000019.9:g.4642508_4642510dup, NC_000019.9:g.4642502_4642510dup

Select item 14912793754.

rs1491279375 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TA [Show Flanks]
Chromosome:: 19:4653770 (GRCh38)
19:4653783 (GRCh37)
Canonical SPDI:: NC_000019.10:4653770:A:ATA
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: ATA=0./0 (ALFA)
AT=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.4653771_4653772insTA, NC_000019.9:g.4653783_4653784insTA, XM_005259487.4:c.*1341_*1342insTA, XM_005259487.3:c.*1341_*1342insTA, NM_152362.3:c.*1341_*1342insTA, NM_152362.2:c.*1341_*1342insTA, XM_011527680.3:c.*1341_*1342insTA, XM_011527680.2:c.*1341_*1342insTA, NM_001167942.1:c.*1341_*1342insTA

Select item 14912730105.

rs1491273010 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 19:4637642 (GRCh38)
19:4637654 (GRCh37)
Canonical SPDI:: NC_000019.10:4637639:GTGT:GT
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.4637640GT[1], NC_000019.9:g.4637652GT[1]

Select item 14912699536.

rs1491269953 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 19:4649889 (GRCh38)
19:4649902 (GRCh37)
Canonical SPDI:: NC_000019.10:4649889::A
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.4649889_4649890insA, NC_000019.9:g.4649901_4649902insA

Select item 14912298137.

rs1491229813 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 19:4653769 (GRCh38)
19:4653781 (GRCh37)
Canonical SPDI:: NC_000019.10:4653768:CA:
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000019.10:g.4653769_4653770del, NC_000019.9:g.4653781_4653782del, XM_005259487.4:c.*1339_*1340del, XM_005259487.3:c.*1339_*1340del, NM_152362.3:c.*1339_*1340del, NM_152362.2:c.*1339_*1340del, XM_011527680.3:c.*1339_*1340del, XM_011527680.2:c.*1339_*1340del, NM_001167942.1:c.*1339_*1340del

Select item 14911756248.

rs1491175624 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 19:4638806 (GRCh38)
19:4638819 (GRCh37)
Canonical SPDI:: NC_000019.10:4638806::G
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.0001/2 (GnomAD)
HGVS:: NC_000019.10:g.4638806_4638807insG, NC_000019.9:g.4638818_4638819insG

Select item 14911343409.

rs1491134340 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 19:4642482 (GRCh38)
19:4642494 (GRCh37)
Canonical SPDI:: NC_000019.10:4642481:CA:
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00025/3 (ALFA)
HGVS:: NC_000019.10:g.4642482_4642483del, NC_000019.9:g.4642494_4642495del

Select item 149111940510.

rs1491119405 [Homo sapiens]

Variant type:: DEL
Alleles:: GG>- [Show Flanks]
Chromosome:: 19:4649889 (GRCh38)
19:4649901 (GRCh37)
Canonical SPDI:: NC_000019.10:4649888:GG:
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.4649889_4649890del, NC_000019.9:g.4649901_4649902del

Select item 149111416311.

rs1491114163 has merged into rs74173015 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:4653781 (GRCh38)
19:4653793 (GRCh37)
Canonical SPDI:: NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:4653769:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.4653781_4653797del, NC_000019.10:g.4653782_4653797del, NC_000019.10:g.4653783_4653797del, NC_000019.10:g.4653784_4653797del, NC_000019.10:g.4653785_4653797del, NC_000019.10:g.4653786_4653797del, NC_000019.10:g.4653787_4653797del, NC_000019.10:g.4653788_4653797del, NC_000019.10:g.4653789_4653797del, NC_000019.10:g.4653790_4653797del, NC_000019.10:g.4653791_4653797del, NC_000019.10:g.4653792_4653797del, NC_000019.10:g.4653793_4653797del, NC_000019.10:g.4653794_4653797del, NC_000019.10:g.4653795_4653797del, NC_000019.10:g.4653796_4653797del, NC_000019.10:g.4653797del, NC_000019.10:g.4653797dup, NC_000019.10:g.4653796_4653797dup, NC_000019.10:g.4653795_4653797dup, NC_000019.10:g.4653794_4653797dup, NC_000019.10:g.4653793_4653797dup, NC_000019.10:g.4653792_4653797dup, NC_000019.10:g.4653790_4653797dup, NC_000019.10:g.4653788_4653797dup, NC_000019.10:g.4653797_4653798insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.4653793_4653809del, NC_000019.9:g.4653794_4653809del, NC_000019.9:g.4653795_4653809del, NC_000019.9:g.4653796_4653809del, NC_000019.9:g.4653797_4653809del, NC_000019.9:g.4653798_4653809del, NC_000019.9:g.4653799_4653809del, NC_000019.9:g.4653800_4653809del, NC_000019.9:g.4653801_4653809del, NC_000019.9:g.4653802_4653809del, NC_000019.9:g.4653803_4653809del, NC_000019.9:g.4653804_4653809del, NC_000019.9:g.4653805_4653809del, NC_000019.9:g.4653806_4653809del, NC_000019.9:g.4653807_4653809del, NC_000019.9:g.4653808_4653809del, NC_000019.9:g.4653809del, NC_000019.9:g.4653809dup, NC_000019.9:g.4653808_4653809dup, NC_000019.9:g.4653807_4653809dup, NC_000019.9:g.4653806_4653809dup, NC_000019.9:g.4653805_4653809dup, NC_000019.9:g.4653804_4653809dup, NC_000019.9:g.4653802_4653809dup, NC_000019.9:g.4653800_4653809dup, NC_000019.9:g.4653809_4653810insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_005259487.4:c.*1351_*1367del, XM_005259487.4:c.*1352_*1367del, XM_005259487.4:c.*1353_*1367del, XM_005259487.4:c.*1354_*1367del, XM_005259487.4:c.*1355_*1367del, XM_005259487.4:c.*1356_*1367del, XM_005259487.4:c.*1357_*1367del, XM_005259487.4:c.*1358_*1367del, XM_005259487.4:c.*1359_*1367del, XM_005259487.4:c.*1360_*1367del, XM_005259487.4:c.*1361_*1367del, XM_005259487.4:c.*1362_*1367del, XM_005259487.4:c.*1363_*1367del, XM_005259487.4:c.*1364_*1367del, XM_005259487.4:c.*1365_*1367del, XM_005259487.4:c.*1366_*1367del, XM_005259487.4:c.*1367del, XM_005259487.4:c.*1367dup, XM_005259487.4:c.*1366_*1367dup, XM_005259487.4:c.*1365_*1367dup, XM_005259487.4:c.*1364_*1367dup, XM_005259487.4:c.*1363_*1367dup, XM_005259487.4:c.*1362_*1367dup, XM_005259487.4:c.*1360_*1367dup, XM_005259487.4:c.*1358_*1367dup, XM_005259487.4:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_005259487.3:c.*1351_*1367del, XM_005259487.3:c.*1352_*1367del, XM_005259487.3:c.*1353_*1367del, XM_005259487.3:c.*1354_*1367del, XM_005259487.3:c.*1355_*1367del, XM_005259487.3:c.*1356_*1367del, XM_005259487.3:c.*1357_*1367del, XM_005259487.3:c.*1358_*1367del, XM_005259487.3:c.*1359_*1367del, XM_005259487.3:c.*1360_*1367del, XM_005259487.3:c.*1361_*1367del, XM_005259487.3:c.*1362_*1367del, XM_005259487.3:c.*1363_*1367del, XM_005259487.3:c.*1364_*1367del, XM_005259487.3:c.*1365_*1367del, XM_005259487.3:c.*1366_*1367del, XM_005259487.3:c.*1367del, XM_005259487.3:c.*1367dup, XM_005259487.3:c.*1366_*1367dup, XM_005259487.3:c.*1365_*1367dup, XM_005259487.3:c.*1364_*1367dup, XM_005259487.3:c.*1363_*1367dup, XM_005259487.3:c.*1362_*1367dup, XM_005259487.3:c.*1360_*1367dup, XM_005259487.3:c.*1358_*1367dup, XM_005259487.3:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_152362.3:c.*1351_*1367del, NM_152362.3:c.*1352_*1367del, NM_152362.3:c.*1353_*1367del, NM_152362.3:c.*1354_*1367del, NM_152362.3:c.*1355_*1367del, NM_152362.3:c.*1356_*1367del, NM_152362.3:c.*1357_*1367del, NM_152362.3:c.*1358_*1367del, NM_152362.3:c.*1359_*1367del, NM_152362.3:c.*1360_*1367del, NM_152362.3:c.*1361_*1367del, NM_152362.3:c.*1362_*1367del, NM_152362.3:c.*1363_*1367del, NM_152362.3:c.*1364_*1367del, NM_152362.3:c.*1365_*1367del, NM_152362.3:c.*1366_*1367del, NM_152362.3:c.*1367del, NM_152362.3:c.*1367dup, NM_152362.3:c.*1366_*1367dup, NM_152362.3:c.*1365_*1367dup, NM_152362.3:c.*1364_*1367dup, NM_152362.3:c.*1363_*1367dup, NM_152362.3:c.*1362_*1367dup, NM_152362.3:c.*1360_*1367dup, NM_152362.3:c.*1358_*1367dup, NM_152362.3:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_152362.2:c.*1351_*1367del, NM_152362.2:c.*1352_*1367del, NM_152362.2:c.*1353_*1367del, NM_152362.2:c.*1354_*1367del, NM_152362.2:c.*1355_*1367del, NM_152362.2:c.*1356_*1367del, NM_152362.2:c.*1357_*1367del, NM_152362.2:c.*1358_*1367del, NM_152362.2:c.*1359_*1367del, NM_152362.2:c.*1360_*1367del, NM_152362.2:c.*1361_*1367del, NM_152362.2:c.*1362_*1367del, NM_152362.2:c.*1363_*1367del, NM_152362.2:c.*1364_*1367del, NM_152362.2:c.*1365_*1367del, NM_152362.2:c.*1366_*1367del, NM_152362.2:c.*1367del, NM_152362.2:c.*1367dup, NM_152362.2:c.*1366_*1367dup, NM_152362.2:c.*1365_*1367dup, NM_152362.2:c.*1364_*1367dup, NM_152362.2:c.*1363_*1367dup, NM_152362.2:c.*1362_*1367dup, NM_152362.2:c.*1360_*1367dup, NM_152362.2:c.*1358_*1367dup, NM_152362.2:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_011527680.3:c.*1351_*1367del, XM_011527680.3:c.*1352_*1367del, XM_011527680.3:c.*1353_*1367del, XM_011527680.3:c.*1354_*1367del, XM_011527680.3:c.*1355_*1367del, XM_011527680.3:c.*1356_*1367del, XM_011527680.3:c.*1357_*1367del, XM_011527680.3:c.*1358_*1367del, XM_011527680.3:c.*1359_*1367del, XM_011527680.3:c.*1360_*1367del, XM_011527680.3:c.*1361_*1367del, XM_011527680.3:c.*1362_*1367del, XM_011527680.3:c.*1363_*1367del, XM_011527680.3:c.*1364_*1367del, XM_011527680.3:c.*1365_*1367del, XM_011527680.3:c.*1366_*1367del, XM_011527680.3:c.*1367del, XM_011527680.3:c.*1367dup, XM_011527680.3:c.*1366_*1367dup, XM_011527680.3:c.*1365_*1367dup, XM_011527680.3:c.*1364_*1367dup, XM_011527680.3:c.*1363_*1367dup, XM_011527680.3:c.*1362_*1367dup, XM_011527680.3:c.*1360_*1367dup, XM_011527680.3:c.*1358_*1367dup, XM_011527680.3:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_011527680.2:c.*1351_*1367del, XM_011527680.2:c.*1352_*1367del, XM_011527680.2:c.*1353_*1367del, XM_011527680.2:c.*1354_*1367del, XM_011527680.2:c.*1355_*1367del, XM_011527680.2:c.*1356_*1367del, XM_011527680.2:c.*1357_*1367del, XM_011527680.2:c.*1358_*1367del, XM_011527680.2:c.*1359_*1367del, XM_011527680.2:c.*1360_*1367del, XM_011527680.2:c.*1361_*1367del, XM_011527680.2:c.*1362_*1367del, XM_011527680.2:c.*1363_*1367del, XM_011527680.2:c.*1364_*1367del, XM_011527680.2:c.*1365_*1367del, XM_011527680.2:c.*1366_*1367del, XM_011527680.2:c.*1367del, XM_011527680.2:c.*1367dup, XM_011527680.2:c.*1366_*1367dup, XM_011527680.2:c.*1365_*1367dup, XM_011527680.2:c.*1364_*1367dup, XM_011527680.2:c.*1363_*1367dup, XM_011527680.2:c.*1362_*1367dup, XM_011527680.2:c.*1360_*1367dup, XM_011527680.2:c.*1358_*1367dup, XM_011527680.2:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001167942.1:c.*1351_*1367del, NM_001167942.1:c.*1352_*1367del, NM_001167942.1:c.*1353_*1367del, NM_001167942.1:c.*1354_*1367del, NM_001167942.1:c.*1355_*1367del, NM_001167942.1:c.*1356_*1367del, NM_001167942.1:c.*1357_*1367del, NM_001167942.1:c.*1358_*1367del, NM_001167942.1:c.*1359_*1367del, NM_001167942.1:c.*1360_*1367del, NM_001167942.1:c.*1361_*1367del, NM_001167942.1:c.*1362_*1367del, NM_001167942.1:c.*1363_*1367del, NM_001167942.1:c.*1364_*1367del, NM_001167942.1:c.*1365_*1367del, NM_001167942.1:c.*1366_*1367del, NM_001167942.1:c.*1367del, NM_001167942.1:c.*1367dup, NM_001167942.1:c.*1366_*1367dup, NM_001167942.1:c.*1365_*1367dup, NM_001167942.1:c.*1364_*1367dup, NM_001167942.1:c.*1363_*1367dup, NM_001167942.1:c.*1362_*1367dup, NM_001167942.1:c.*1360_*1367dup, NM_001167942.1:c.*1358_*1367dup, NM_001167942.1:c.*1367_*1368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149104688312.

rs1491046883 [Homo sapiens]

Variant type:: INS
Alleles:: ->G,T [Show Flanks]
Chromosome:: 19:4642497 (GRCh38)
19:4642510 (GRCh37)
Canonical SPDI:: NC_000019.10:4642497::G,NC_000019.10:4642497::T
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00003/4 (GnomAD)
G=0.000036/1 (TOMMO)
HGVS:: NC_000019.10:g.4642497_4642498insG, NC_000019.10:g.4642497_4642498insT, NC_000019.9:g.4642509_4642510insG, NC_000019.9:g.4642509_4642510insT

Select item 149098700013.

rs1490987000 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:4646156 (GRCh38)
19:4646168 (GRCh37)
Canonical SPDI:: NC_000019.10:4646155:T:C
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.4646156T>C, NC_000019.9:g.4646168T>C

Select item 149081154214.

rs1490811542 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:4639584 (GRCh38)
19:4639596 (GRCh37)
Canonical SPDI:: NC_000019.10:4639583:G:T
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000312/2 (1000Genomes)
HGVS:: NC_000019.10:g.4639584G>T, NC_000019.9:g.4639596G>T, NM_152362.3:c.-49G>T, NM_152362.2:c.-49G>T, XM_011527680.3:c.-45G>T, XM_011527680.2:c.-45G>T, XM_011527680.1:c.-45G>T

Select item 149032234515.

rs1490322345 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:4640042 (GRCh38)
19:4640054 (GRCh37)
Canonical SPDI:: NC_000019.10:4640041:G:A
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000019.10:g.4640042G>A, NC_000019.9:g.4640054G>A, NM_001167942.1:c.-121G>A

Select item 149029511116.

rs1490295111 [Homo sapiens]

Variant type:: DELINS
Alleles:: GCCG>- [Show Flanks]
Chromosome:: 19:4646285 (GRCh38)
19:4646297 (GRCh37)
Canonical SPDI:: NC_000019.10:4646281:CCGGCCG:CCG
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.4646285_4646288del, NC_000019.9:g.4646297_4646300del

Select item 148995700717.

rs1489957007 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:4644550 (GRCh38)
19:4644562 (GRCh37)
Canonical SPDI:: NC_000019.10:4644549:A:G
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.4644550A>G, NC_000019.9:g.4644562A>G

Select item 148983353818.

rs1489833538 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:4640610 (GRCh38)
19:4640622 (GRCh37)
Canonical SPDI:: NC_000019.10:4640609:C:G
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.4640610C>G, NC_000019.9:g.4640622C>G

Select item 148982027319.

rs1489820273 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:4647340 (GRCh38)
19:4647352 (GRCh37)
Canonical SPDI:: NC_000019.10:4647339:A:C
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000108/2 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
C=0.000446/2 (Estonian)
HGVS:: NC_000019.10:g.4647340A>C, NC_000019.9:g.4647352A>C

Select item 148976817520.

rs1489768175 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:4641393 (GRCh38)
19:4641405 (GRCh37)
Canonical SPDI:: NC_000019.10:4641392:G:T
Gene:: TNFAIP8L1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.4641393G>T, NC_000019.9:g.4641405G>T

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