SNP Links for Nucleotide (Select 383209646) - SNP

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Select item 14915842361.

rs1491584236 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCTA>-,TCTATCTA [Show Flanks]
Chromosome:: 17:7672635 (GRCh38)
17:7575953 (GRCh37)
Canonical SPDI:: NC_000017.11:7672626:TCTATCTATCTA:TCTATCTA,NC_000017.11:7672626:TCTATCTATCTA:TCTATCTATCTATCTA
Gene:: TP53 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTATCTATCTATCTA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.7672627TCTA[2], NC_000017.11:g.7672627TCTA[4], NC_000017.10:g.7575945TCTA[2], NC_000017.10:g.7575945TCTA[4], NG_017013.2:g.19913TAGA[2], NG_017013.2:g.19913TAGA[4]

Select item 14915745042.

rs1491574504 [Homo sapiens]

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

Select item 14915602033.

rs1491560203 has merged into rs67602984 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 17:7665390 (GRCh38)
17:7568708 (GRCh37)
Canonical SPDI:: NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000017.11:g.7665390_7665400del, NC_000017.11:g.7665395_7665400del, NC_000017.11:g.7665396_7665400del, NC_000017.11:g.7665397_7665400del, NC_000017.11:g.7665398_7665400del, NC_000017.11:g.7665399_7665400del, NC_000017.11:g.7665400del, NC_000017.11:g.7665400dup, NC_000017.11:g.7665399_7665400dup, NC_000017.11:g.7665398_7665400dup, NC_000017.11:g.7665397_7665400dup, NC_000017.11:g.7665396_7665400dup, NC_000017.11:g.7665395_7665400dup, NC_000017.11:g.7665394_7665400dup, NC_000017.11:g.7665393_7665400dup, NC_000017.11:g.7665392_7665400dup, NC_000017.11:g.7665391_7665400dup, NC_000017.11:g.7665390_7665400dup, NC_000017.11:g.7665389_7665400dup, NC_000017.11:g.7665388_7665400dup, NC_000017.11:g.7665387_7665400dup, NC_000017.11:g.7665386_7665400dup, NC_000017.11:g.7665385_7665400dup, NC_000017.11:g.7665384_7665400dup, NC_000017.11:g.7665380_7665400A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.11:g.7665380_7665400A[22]CCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.11:g.7665380_7665400A[22]CCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.10:g.7568708_7568718del, NC_000017.10:g.7568713_7568718del, NC_000017.10:g.7568714_7568718del, NC_000017.10:g.7568715_7568718del, NC_000017.10:g.7568716_7568718del, NC_000017.10:g.7568717_7568718del, NC_000017.10:g.7568718del, NC_000017.10:g.7568718dup, NC_000017.10:g.7568717_7568718dup, NC_000017.10:g.7568716_7568718dup, NC_000017.10:g.7568715_7568718dup, NC_000017.10:g.7568714_7568718dup, NC_000017.10:g.7568713_7568718dup, NC_000017.10:g.7568712_7568718dup, NC_000017.10:g.7568711_7568718dup, NC_000017.10:g.7568710_7568718dup, NC_000017.10:g.7568709_7568718dup, NC_000017.10:g.7568708_7568718dup, NC_000017.10:g.7568707_7568718dup, NC_000017.10:g.7568706_7568718dup, NC_000017.10:g.7568705_7568718dup, NC_000017.10:g.7568704_7568718dup, NC_000017.10:g.7568703_7568718dup, NC_000017.10:g.7568702_7568718dup, NC_000017.10:g.7568698_7568718A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.10:g.7568698_7568718A[22]CCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.10:g.7568698_7568718A[22]CCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_017013.2:g.27161_27171del, NG_017013.2:g.27166_27171del, NG_017013.2:g.27167_27171del, NG_017013.2:g.27168_27171del, NG_017013.2:g.27169_27171del, NG_017013.2:g.27170_27171del, NG_017013.2:g.27171del, NG_017013.2:g.27171dup, NG_017013.2:g.27170_27171dup, NG_017013.2:g.27169_27171dup, NG_017013.2:g.27168_27171dup, NG_017013.2:g.27167_27171dup, NG_017013.2:g.27166_27171dup, NG_017013.2:g.27165_27171dup, NG_017013.2:g.27164_27171dup, NG_017013.2:g.27163_27171dup, NG_017013.2:g.27162_27171dup, NG_017013.2:g.27161_27171dup, NG_017013.2:g.27160_27171dup, NG_017013.2:g.27159_27171dup, NG_017013.2:g.27158_27171dup, NG_017013.2:g.27157_27171dup, NG_017013.2:g.27156_27171dup, NG_017013.2:g.27155_27171dup, NG_017013.2:g.27151_27171T[33]GTTTTTTTTTTTTTTTTTTTTTT[1], NG_017013.2:g.27151_27171T[32]GGTTTTTTTTTTTTTTTTTTTTTT[1], NG_017013.2:g.27151_27171T[32]GTGGTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14915367994.

rs1491536799 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTTTTTGTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 17:7681171 (GRCh38)
17:7584490 (GRCh37)
Canonical SPDI:: NC_000017.11:7681171:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTT
Gene:: TP53 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by cluster
HGVS:: NC_000017.11:g.7681172_7681188T[23]GTTTTTTTTTTTTTTTTT[1], NC_000017.10:g.7584490_7584506T[23]GTTTTTTTTTTTTTTTTT[1], NG_017013.2:g.11363_11379A[17]CAAAAAAAAAAAAAAAAAAAAAAA[1], NG_028245.1:g.102_118T[23]GTTTTTTTTTTTTTTTTT[1]

Select item 14914530185.

rs1491453018 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 17:7672628 (GRCh38)
17:7575946 (GRCh37)
Canonical SPDI:: NC_000017.11:7672625:CTCT:CT
Gene:: TP53 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CTCT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.7672626CT[1], NC_000017.10:g.7575944CT[1], NG_017013.2:g.19922AG[1]

Select item 14914315466.

rs1491431546 [Homo sapiens]

Variant type:: DEL
Alleles:: AC>- [Show Flanks]
Chromosome:: 17:7665400 (GRCh38)
17:7568718 (GRCh37)
Canonical SPDI:: NC_000017.11:7665399:AC:
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000017.11:g.7665400_7665401del, NC_000017.10:g.7568718_7568719del, NG_017013.2:g.27150_27151del

Select item 14914252907.

rs1491425290 has merged into rs67602984 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 17:7665390 (GRCh38)
17:7568708 (GRCh37)
Canonical SPDI:: NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7665379:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000017.11:g.7665390_7665400del, NC_000017.11:g.7665395_7665400del, NC_000017.11:g.7665396_7665400del, NC_000017.11:g.7665397_7665400del, NC_000017.11:g.7665398_7665400del, NC_000017.11:g.7665399_7665400del, NC_000017.11:g.7665400del, NC_000017.11:g.7665400dup, NC_000017.11:g.7665399_7665400dup, NC_000017.11:g.7665398_7665400dup, NC_000017.11:g.7665397_7665400dup, NC_000017.11:g.7665396_7665400dup, NC_000017.11:g.7665395_7665400dup, NC_000017.11:g.7665394_7665400dup, NC_000017.11:g.7665393_7665400dup, NC_000017.11:g.7665392_7665400dup, NC_000017.11:g.7665391_7665400dup, NC_000017.11:g.7665390_7665400dup, NC_000017.11:g.7665389_7665400dup, NC_000017.11:g.7665388_7665400dup, NC_000017.11:g.7665387_7665400dup, NC_000017.11:g.7665386_7665400dup, NC_000017.11:g.7665385_7665400dup, NC_000017.11:g.7665384_7665400dup, NC_000017.11:g.7665380_7665400A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.11:g.7665380_7665400A[22]CCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.11:g.7665380_7665400A[22]CCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.10:g.7568708_7568718del, NC_000017.10:g.7568713_7568718del, NC_000017.10:g.7568714_7568718del, NC_000017.10:g.7568715_7568718del, NC_000017.10:g.7568716_7568718del, NC_000017.10:g.7568717_7568718del, NC_000017.10:g.7568718del, NC_000017.10:g.7568718dup, NC_000017.10:g.7568717_7568718dup, NC_000017.10:g.7568716_7568718dup, NC_000017.10:g.7568715_7568718dup, NC_000017.10:g.7568714_7568718dup, NC_000017.10:g.7568713_7568718dup, NC_000017.10:g.7568712_7568718dup, NC_000017.10:g.7568711_7568718dup, NC_000017.10:g.7568710_7568718dup, NC_000017.10:g.7568709_7568718dup, NC_000017.10:g.7568708_7568718dup, NC_000017.10:g.7568707_7568718dup, NC_000017.10:g.7568706_7568718dup, NC_000017.10:g.7568705_7568718dup, NC_000017.10:g.7568704_7568718dup, NC_000017.10:g.7568703_7568718dup, NC_000017.10:g.7568702_7568718dup, NC_000017.10:g.7568698_7568718A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.10:g.7568698_7568718A[22]CCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.10:g.7568698_7568718A[22]CCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_017013.2:g.27161_27171del, NG_017013.2:g.27166_27171del, NG_017013.2:g.27167_27171del, NG_017013.2:g.27168_27171del, NG_017013.2:g.27169_27171del, NG_017013.2:g.27170_27171del, NG_017013.2:g.27171del, NG_017013.2:g.27171dup, NG_017013.2:g.27170_27171dup, NG_017013.2:g.27169_27171dup, NG_017013.2:g.27168_27171dup, NG_017013.2:g.27167_27171dup, NG_017013.2:g.27166_27171dup, NG_017013.2:g.27165_27171dup, NG_017013.2:g.27164_27171dup, NG_017013.2:g.27163_27171dup, NG_017013.2:g.27162_27171dup, NG_017013.2:g.27161_27171dup, NG_017013.2:g.27160_27171dup, NG_017013.2:g.27159_27171dup, NG_017013.2:g.27158_27171dup, NG_017013.2:g.27157_27171dup, NG_017013.2:g.27156_27171dup, NG_017013.2:g.27155_27171dup, NG_017013.2:g.27151_27171T[33]GTTTTTTTTTTTTTTTTTTTTTT[1], NG_017013.2:g.27151_27171T[32]GGTTTTTTTTTTTTTTTTTTTTTT[1], NG_017013.2:g.27151_27171T[32]GTGGTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14913793448.

rs1491379344 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 17:7665379 (GRCh38)
17:7568697 (GRCh37)
Canonical SPDI:: NC_000017.11:7665378:CA:
Validated:: by frequency,by alfa
MAF:: -=0.01391/165 (ALFA)
HGVS:: NC_000017.11:g.7665379_7665380del, NC_000017.10:g.7568697_7568698del, NG_017013.2:g.27171_27172del

Select item 14913462399.

rs1491346239 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 17:7661037 (GRCh38)
17:7564356 (GRCh37)
Canonical SPDI:: NC_000017.11:7661037:C:CC
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000017.11:g.7661038dup, NC_000017.10:g.7564356dup, NG_017013.2:g.31513dup

Select item 149132943410.

rs1491329434 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 17:7691392 (GRCh38)
17:7594710 (GRCh37)
Canonical SPDI:: NC_000017.11:7691389:GTGT:GT
Gene:: WRAP53 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGT=0./0 (ALFA)
-=0.000015/2 (GnomAD)
-=0.000019/5 (TOPMED)
HGVS:: NC_000017.11:g.7691390GT[1], NC_000017.10:g.7594708GT[1], NG_017013.2:g.1158AC[1], NG_028245.1:g.10320GT[1]

Select item 149132615011.

rs1491326150 [Homo sapiens]

Variant type:: INS
Alleles:: ->AC,AG,G [Show Flanks]
Chromosome:: 17:7665400 (GRCh38)
17:7568719 (GRCh37)
Canonical SPDI:: NC_000017.11:7665400::AC,NC_000017.11:7665400::AG,NC_000017.11:7665400::G
Validated:: by frequency,by alfa
MAF:: AG=0./0 (ALFA)
HGVS:: NC_000017.11:g.7665400_7665401insAC, NC_000017.11:g.7665400_7665401insAG, NC_000017.11:g.7665400_7665401insG, NC_000017.10:g.7568718_7568719insAC, NC_000017.10:g.7568718_7568719insAG, NC_000017.10:g.7568718_7568719insG, NG_017013.2:g.27150_27151insGT, NG_017013.2:g.27150_27151insCT, NG_017013.2:g.27150_27151insC

Select item 149128454312.

rs1491284543 has merged into rs34199921 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 17:7681181 (GRCh38)
17:7584499 (GRCh37)
Canonical SPDI:: NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000017.11:7681170:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TP53 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.02508/15 (NorthernSweden)
-=0.41234/2065 (1000Genomes)
HGVS:: NC_000017.11:g.7681181_7681188del, NC_000017.11:g.7681182_7681188del, NC_000017.11:g.7681183_7681188del, NC_000017.11:g.7681184_7681188del, NC_000017.11:g.7681185_7681188del, NC_000017.11:g.7681186_7681188del, NC_000017.11:g.7681187_7681188del, NC_000017.11:g.7681188del, NC_000017.11:g.7681188dup, NC_000017.11:g.7681187_7681188dup, NC_000017.11:g.7681186_7681188dup, NC_000017.11:g.7681185_7681188dup, NC_000017.11:g.7681181_7681188dup, NC_000017.11:g.7681175_7681188dup, NC_000017.10:g.7584499_7584506del, NC_000017.10:g.7584500_7584506del, NC_000017.10:g.7584501_7584506del, NC_000017.10:g.7584502_7584506del, NC_000017.10:g.7584503_7584506del, NC_000017.10:g.7584504_7584506del, NC_000017.10:g.7584505_7584506del, NC_000017.10:g.7584506del, NC_000017.10:g.7584506dup, NC_000017.10:g.7584505_7584506dup, NC_000017.10:g.7584504_7584506dup, NC_000017.10:g.7584503_7584506dup, NC_000017.10:g.7584499_7584506dup, NC_000017.10:g.7584493_7584506dup, NG_017013.2:g.11373_11380del, NG_017013.2:g.11374_11380del, NG_017013.2:g.11375_11380del, NG_017013.2:g.11376_11380del, NG_017013.2:g.11377_11380del, NG_017013.2:g.11378_11380del, NG_017013.2:g.11379_11380del, NG_017013.2:g.11380del, NG_017013.2:g.11380dup, NG_017013.2:g.11379_11380dup, NG_017013.2:g.11378_11380dup, NG_017013.2:g.11377_11380dup, NG_017013.2:g.11373_11380dup, NG_017013.2:g.11367_11380dup, NG_028245.1:g.111_118del, NG_028245.1:g.112_118del, NG_028245.1:g.113_118del, NG_028245.1:g.114_118del, NG_028245.1:g.115_118del, NG_028245.1:g.116_118del, NG_028245.1:g.117_118del, NG_028245.1:g.118del, NG_028245.1:g.118dup, NG_028245.1:g.117_118dup, NG_028245.1:g.116_118dup, NG_028245.1:g.115_118dup, NG_028245.1:g.111_118dup, NG_028245.1:g.105_118dup

Select item 149127328413.

rs1491273284 has merged into rs869152334 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 17:7660509 (GRCh38)
17:7563827 (GRCh37)
Canonical SPDI:: NC_000017.11:7660507:ACA:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000017.11:g.7660509_7660510del, NC_000017.10:g.7563827_7563828del, NG_017013.2:g.32042_32043del

Select item 149126708114.

rs1491267081 [Homo sapiens]

Variant type:: DELINS
Alleles:: TC>- [Show Flanks]
Chromosome:: 17:7661039 (GRCh38)
17:7564357 (GRCh37)
Canonical SPDI:: NC_000017.11:7661036:TCTC:TC
Validated:: by frequency,by alfa
MAF:: TCTC=0./0 (ALFA)
HGVS:: NC_000017.11:g.7661037TC[1], NC_000017.10:g.7564355TC[1], NG_017013.2:g.31511GA[1]

Select item 149112658515.

rs1491126585 [Homo sapiens]

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

Select item 149107914316.

rs1491079143 has merged into rs34308401 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 17:7673134 (GRCh38)
17:7576452 (GRCh37)
Canonical SPDI:: NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:7673125:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TP53 (Varview)
Functional Consequence:: intron_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.7673134_7673144del, NC_000017.11:g.7673136_7673144del, NC_000017.11:g.7673139_7673144del, NC_000017.11:g.7673140_7673144del, NC_000017.11:g.7673142_7673144del, NC_000017.11:g.7673143_7673144del, NC_000017.11:g.7673144del, NC_000017.11:g.7673144dup, NC_000017.11:g.7673143_7673144dup, NC_000017.11:g.7673142_7673144dup, NC_000017.11:g.7673141_7673144dup, NC_000017.11:g.7673140_7673144dup, NC_000017.11:g.7673139_7673144dup, NC_000017.11:g.7673138_7673144dup, NC_000017.11:g.7673137_7673144dup, NC_000017.11:g.7673134_7673144dup, NC_000017.11:g.7673130_7673144dup, NC_000017.10:g.7576452_7576462del, NC_000017.10:g.7576454_7576462del, NC_000017.10:g.7576457_7576462del, NC_000017.10:g.7576458_7576462del, NC_000017.10:g.7576460_7576462del, NC_000017.10:g.7576461_7576462del, NC_000017.10:g.7576462del, NC_000017.10:g.7576462dup, NC_000017.10:g.7576461_7576462dup, NC_000017.10:g.7576460_7576462dup, NC_000017.10:g.7576459_7576462dup, NC_000017.10:g.7576458_7576462dup, NC_000017.10:g.7576457_7576462dup, NC_000017.10:g.7576456_7576462dup, NC_000017.10:g.7576455_7576462dup, NC_000017.10:g.7576452_7576462dup, NC_000017.10:g.7576448_7576462dup, NG_017013.2:g.19415_19425del, NG_017013.2:g.19417_19425del, NG_017013.2:g.19420_19425del, NG_017013.2:g.19421_19425del, NG_017013.2:g.19423_19425del, NG_017013.2:g.19424_19425del, NG_017013.2:g.19425del, NG_017013.2:g.19425dup, NG_017013.2:g.19424_19425dup, NG_017013.2:g.19423_19425dup, NG_017013.2:g.19422_19425dup, NG_017013.2:g.19421_19425dup, NG_017013.2:g.19420_19425dup, NG_017013.2:g.19419_19425dup, NG_017013.2:g.19418_19425dup, NG_017013.2:g.19415_19425dup, NG_017013.2:g.19411_19425dup

Select item 149105022817.

rs1491050228 has merged into rs34103303 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA [Show Flanks]
Chromosome:: 17:7667267 (GRCh38)
17:7570585 (GRCh37)
Canonical SPDI:: NC_000017.11:7667260:AAAAAAAAAAAAA:AAAAAA,NC_000017.11:7667260:AAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:7667260:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000017.11:7667260:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000017.11:7667260:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:7667260:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:7667260:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
A=0.2857/1431 (1000Genomes)
HGVS:: NC_000017.11:g.7667267_7667273del, NC_000017.11:g.7667271_7667273del, NC_000017.11:g.7667272_7667273del, NC_000017.11:g.7667273del, NC_000017.11:g.7667273dup, NC_000017.11:g.7667272_7667273dup, NC_000017.11:g.7667271_7667273dup, NC_000017.10:g.7570585_7570591del, NC_000017.10:g.7570589_7570591del, NC_000017.10:g.7570590_7570591del, NC_000017.10:g.7570591del, NC_000017.10:g.7570591dup, NC_000017.10:g.7570590_7570591dup, NC_000017.10:g.7570589_7570591dup, NG_017013.2:g.25284_25290del, NG_017013.2:g.25288_25290del, NG_017013.2:g.25289_25290del, NG_017013.2:g.25290del, NG_017013.2:g.25290dup, NG_017013.2:g.25289_25290dup, NG_017013.2:g.25288_25290dup

Select item 149094927218.

rs1490949272 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:7679913 (GRCh38)
17:7583231 (GRCh37)
Canonical SPDI:: NC_000017.11:7679912:G:A
Gene:: TP53 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.7679913G>A, NC_000017.10:g.7583231G>A, NG_017013.2:g.12638C>T

Select item 149093143719.

rs1490931437 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:7673260 (GRCh38)
17:7576578 (GRCh37)
Canonical SPDI:: NC_000017.11:7673259:G:A
Gene:: TP53 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
Validated:: by cluster
HGVS:: NC_000017.11:g.7673260G>A, NC_000017.10:g.7576578G>A, NG_017013.2:g.19291C>T, NM_001276696.3:c.*47C>T, NM_001276696.2:c.*47C>T, NM_001276696.1:c.*47C>T, NM_001126114.3:c.*47C>T, NM_001126114.2:c.*47C>T, NM_001276695.3:c.883C>T, NM_001276695.2:c.883C>T, NM_001276695.1:c.883C>T, NM_001126113.3:c.1000C>T, NM_001126113.2:c.1000C>T, NM_001276698.3:c.*47C>T, NM_001276698.2:c.*47C>T, NM_001276698.1:c.*47C>T, NM_001276699.3:c.523C>T, NM_001276699.2:c.523C>T, NM_001276699.1:c.523C>T, NM_001126116.2:c.*47C>T, NM_001126116.1:c.*47C>T, NM_001126117.2:c.604C>T, NM_001126117.1:c.604C>T, NM_001407271.1:c.*47C>T, NM_001407270.1:c.*47C>T, NM_001407269.1:c.*47C>T, NM_001407268.1:c.*47C>T, NP_001263624.1:p.Leu295Phe, NP_001119585.1:p.Leu334Phe, NP_001263628.1:p.Leu175Phe, NP_001119589.1:p.Leu202Phe

Select item 149092986820.

rs1490929868 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:7666673 (GRCh38)
17:7569991 (GRCh37)
Canonical SPDI:: NC_000017.11:7666672:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.7666673C>T, NC_000017.10:g.7569991C>T, NG_017013.2:g.25878G>A

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