SNP Links for Gene (Select 84896) - SNP

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Select item 14915391821.

rs1491539182 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,T [Show Flanks]
Chromosome:: 10:87798622 (GRCh38)
10:89558380 (GRCh37)
Canonical SPDI:: NC_000010.11:87798622::A,NC_000010.11:87798622::T
Gene:: ATAD1 (Varview), LOC124902476 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00003/4 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.87798622_87798623insA, NC_000010.11:g.87798622_87798623insT, NC_000010.10:g.89558379_89558380insA, NC_000010.10:g.89558379_89558380insT, NW_013171807.1:g.14444_14445insA, NW_013171807.1:g.14444_14445insT

Select item 14915363892.

rs1491536389 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 10:87822305 (GRCh38)
10:89582063 (GRCh37)
Canonical SPDI:: NC_000010.11:87822305:T:TT
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.87822306dup, NC_000010.10:g.89582063dup, NW_013171807.1:g.38128dup

Select item 14914580003.

rs1491458000 has merged into rs748674665 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA [Show Flanks]
Chromosome:: 10:87799798 (GRCh38)
10:89559555 (GRCh37)
Canonical SPDI:: NC_000010.11:87799794:AAAAA:AAA,NC_000010.11:87799794:AAAAA:AAAA,NC_000010.11:87799794:AAAAA:AAAAAA
Gene:: ATAD1 (Varview), LOC124902476 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0./0 (ALFA)
-=0.00012/2 (TOMMO)
HGVS:: NC_000010.11:g.87799798_87799799del, NC_000010.11:g.87799799del, NC_000010.11:g.87799799dup, NC_000010.10:g.89559555_89559556del, NC_000010.10:g.89559556del, NC_000010.10:g.89559556dup, NW_013171807.1:g.15620_15621del, NW_013171807.1:g.15621del, NW_013171807.1:g.15621dup

Select item 14914395944.

rs1491439594 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:87838461 (GRCh38)
10:89598218 (GRCh37)
Canonical SPDI:: NC_000010.11:87838460:CA:
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.87838461_87838462del, NC_000010.10:g.89598218_89598219del, NW_013171807.1:g.54283_54284del

Select item 14913074275.

rs1491307427 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 10:87757286 (GRCh38)
10:89517044 (GRCh37)
Canonical SPDI:: NC_000010.11:87757286::C
Gene:: ATAD1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.87757286_87757287insC, NC_000010.10:g.89517043_89517044insC

Select item 14912930456.

rs1491293045 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:87822307 (GRCh38)
10:89582064 (GRCh37)
Canonical SPDI:: NC_000010.11:87822304:ATAT:AT
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATAT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.87822305AT[1], NC_000010.10:g.89582062AT[1], NW_013171807.1:g.38127AT[1]

Select item 14912699147.

rs1491269914 has merged into rs33991078 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:87791219 (GRCh38)
10:89550976 (GRCh37)
Canonical SPDI:: NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87791204:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ATAD1 (Varview), LOC124902476 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.3255/1630 (1000Genomes)
HGVS:: NC_000010.11:g.87791219_87791222del, NC_000010.11:g.87791220_87791222del, NC_000010.11:g.87791221_87791222del, NC_000010.11:g.87791222del, NC_000010.11:g.87791222dup, NC_000010.11:g.87791221_87791222dup, NC_000010.11:g.87791220_87791222dup, NC_000010.11:g.87791219_87791222dup, NC_000010.11:g.87791215_87791222dup, NC_000010.10:g.89550976_89550979del, NC_000010.10:g.89550977_89550979del, NC_000010.10:g.89550978_89550979del, NC_000010.10:g.89550979del, NC_000010.10:g.89550979dup, NC_000010.10:g.89550978_89550979dup, NC_000010.10:g.89550977_89550979dup, NC_000010.10:g.89550976_89550979dup, NC_000010.10:g.89550972_89550979dup, NW_013171807.1:g.7041_7044del, NW_013171807.1:g.7042_7044del, NW_013171807.1:g.7043_7044del, NW_013171807.1:g.7044del, NW_013171807.1:g.7044dup, NW_013171807.1:g.7043_7044dup, NW_013171807.1:g.7042_7044dup, NW_013171807.1:g.7041_7044dup, NW_013171807.1:g.7037_7044dup

Select item 14912678188.

rs1491267818 has merged into rs112302394 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCTCTCTCTC>-,TC,TCTC,TCTCTC,TCTCTCTC,TCTCTCTCTCTC,TCTCTCTCTCTCTC,TCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTC [Show Flanks]
Chromosome:: 10:87838751 (GRCh38)
10:89598508 (GRCh37)
Canonical SPDI:: NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000010.11:87838736:TCTCTCTCTCTCTCTCTCTCTCTC:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCTCTCTCTCTCTC=0./0 (ALFA)
-=0.0088/5 (NorthernSweden)
TC=0.02396/120 (1000Genomes)
-=0.0801/297 (TWINSUK)
-=0.08848/341 (ALSPAC)
HGVS:: NC_000010.11:g.87838737TC[7], NC_000010.11:g.87838737TC[8], NC_000010.11:g.87838737TC[9], NC_000010.11:g.87838737TC[10], NC_000010.11:g.87838737TC[11], NC_000010.11:g.87838737TC[13], NC_000010.11:g.87838737TC[14], NC_000010.11:g.87838737TC[15], NC_000010.11:g.87838737TC[16], NC_000010.10:g.89598494TC[7], NC_000010.10:g.89598494TC[8], NC_000010.10:g.89598494TC[9], NC_000010.10:g.89598494TC[10], NC_000010.10:g.89598494TC[11], NC_000010.10:g.89598494TC[13], NC_000010.10:g.89598494TC[14], NC_000010.10:g.89598494TC[15], NC_000010.10:g.89598494TC[16], NW_013171807.1:g.54559TC[7], NW_013171807.1:g.54559TC[8], NW_013171807.1:g.54559TC[9], NW_013171807.1:g.54559TC[10], NW_013171807.1:g.54559TC[11], NW_013171807.1:g.54559TC[13], NW_013171807.1:g.54559TC[14], NW_013171807.1:g.54559TC[15], NW_013171807.1:g.54559TC[16]

Select item 14912675339.

rs1491267533 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TT [Show Flanks]
Chromosome:: 10:87833726 (GRCh38)
10:89593484 (GRCh37)
Canonical SPDI:: NC_000010.11:87833726::T,NC_000010.11:87833726::TT
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.00026/4 (ALFA)
HGVS:: NC_000010.11:g.87833726_87833727insT, NC_000010.11:g.87833726_87833727insTT, NC_000010.10:g.89593483_89593484insT, NC_000010.10:g.89593483_89593484insTT, NW_013171807.1:g.49548_49549insT, NW_013171807.1:g.49548_49549insTT

Select item 149115686110.

rs1491156861 [Homo sapiens]

Variant type:: DEL
Alleles:: CC>- [Show Flanks]
Chromosome:: 10:87833726 (GRCh38)
10:89593483 (GRCh37)
Canonical SPDI:: NC_000010.11:87833725:CC:
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.87833726_87833727del, NC_000010.10:g.89593483_89593484del, NW_013171807.1:g.49548_49549del

Select item 149115545611.

rs1491155456 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:87791204 (GRCh38)
10:89550961 (GRCh37)
Canonical SPDI:: NC_000010.11:87791203:CA:
Gene:: ATAD1 (Varview), LOC124902476 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00025/3 (ALFA)
HGVS:: NC_000010.11:g.87791204_87791205del, NC_000010.10:g.89550961_89550962del, NW_013171807.1:g.7026_7027del

Select item 149113287112.

rs1491132871 has merged into rs770282016 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:87838471 (GRCh38)
10:89598228 (GRCh37)
Canonical SPDI:: NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:87838461:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0./0 (GENOME_DK)
-=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.87838471_87838488del, NC_000010.11:g.87838474_87838488del, NC_000010.11:g.87838475_87838488del, NC_000010.11:g.87838476_87838488del, NC_000010.11:g.87838477_87838488del, NC_000010.11:g.87838478_87838488del, NC_000010.11:g.87838479_87838488del, NC_000010.11:g.87838480_87838488del, NC_000010.11:g.87838481_87838488del, NC_000010.11:g.87838482_87838488del, NC_000010.11:g.87838483_87838488del, NC_000010.11:g.87838484_87838488del, NC_000010.11:g.87838485_87838488del, NC_000010.11:g.87838486_87838488del, NC_000010.11:g.87838487_87838488del, NC_000010.11:g.87838488del, NC_000010.11:g.87838488dup, NC_000010.11:g.87838487_87838488dup, NC_000010.11:g.87838486_87838488dup, NC_000010.11:g.87838485_87838488dup, NC_000010.11:g.87838484_87838488dup, NC_000010.11:g.87838483_87838488dup, NC_000010.11:g.87838482_87838488dup, NC_000010.11:g.87838481_87838488dup, NC_000010.11:g.87838480_87838488dup, NC_000010.11:g.87838479_87838488dup, NC_000010.10:g.89598228_89598245del, NC_000010.10:g.89598231_89598245del, NC_000010.10:g.89598232_89598245del, NC_000010.10:g.89598233_89598245del, NC_000010.10:g.89598234_89598245del, NC_000010.10:g.89598235_89598245del, NC_000010.10:g.89598236_89598245del, NC_000010.10:g.89598237_89598245del, NC_000010.10:g.89598238_89598245del, NC_000010.10:g.89598239_89598245del, NC_000010.10:g.89598240_89598245del, NC_000010.10:g.89598241_89598245del, NC_000010.10:g.89598242_89598245del, NC_000010.10:g.89598243_89598245del, NC_000010.10:g.89598244_89598245del, NC_000010.10:g.89598245del, NC_000010.10:g.89598245dup, NC_000010.10:g.89598244_89598245dup, NC_000010.10:g.89598243_89598245dup, NC_000010.10:g.89598242_89598245dup, NC_000010.10:g.89598241_89598245dup, NC_000010.10:g.89598240_89598245dup, NC_000010.10:g.89598239_89598245dup, NC_000010.10:g.89598238_89598245dup, NC_000010.10:g.89598237_89598245dup, NC_000010.10:g.89598236_89598245dup, NW_013171807.1:g.54293_54310del, NW_013171807.1:g.54296_54310del, NW_013171807.1:g.54297_54310del, NW_013171807.1:g.54298_54310del, NW_013171807.1:g.54299_54310del, NW_013171807.1:g.54300_54310del, NW_013171807.1:g.54301_54310del, NW_013171807.1:g.54302_54310del, NW_013171807.1:g.54303_54310del, NW_013171807.1:g.54304_54310del, NW_013171807.1:g.54305_54310del, NW_013171807.1:g.54306_54310del, NW_013171807.1:g.54307_54310del, NW_013171807.1:g.54308_54310del, NW_013171807.1:g.54309_54310del, NW_013171807.1:g.54310del, NW_013171807.1:g.54310dup, NW_013171807.1:g.54309_54310dup, NW_013171807.1:g.54308_54310dup, NW_013171807.1:g.54307_54310dup, NW_013171807.1:g.54306_54310dup, NW_013171807.1:g.54305_54310dup, NW_013171807.1:g.54304_54310dup, NW_013171807.1:g.54303_54310dup, NW_013171807.1:g.54302_54310dup, NW_013171807.1:g.54301_54310dup

Select item 149097245213.

rs1490972452 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:87811592 (GRCh38)
10:89571349 (GRCh37)
Canonical SPDI:: NC_000010.11:87811591:C:A
Gene:: ATAD1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.87811592C>A, NC_000010.10:g.89571349C>A, NW_013171807.1:g.27414C>A

Select item 149093225614.

rs1490932256 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:87754671 (GRCh38)
10:89514428 (GRCh37)
Canonical SPDI:: NC_000010.11:87754670:C:A,NC_000010.11:87754670:C:T
Gene:: ATAD1 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.87754671C>A, NC_000010.11:g.87754671C>T, NC_000010.10:g.89514428C>A, NC_000010.10:g.89514428C>T, XM_005270252.6:c.*16G>T, XM_005270252.6:c.*16G>A, XM_005270252.5:c.*16G>T, XM_005270252.5:c.*16G>A, XM_005270252.4:c.*16G>T, XM_005270252.4:c.*16G>A, XM_005270252.3:c.*16G>T, XM_005270252.3:c.*16G>A, XM_005270252.2:c.*16G>T, XM_005270252.2:c.*16G>A, XM_005270252.1:c.*16G>T, XM_005270252.1:c.*16G>A, NM_032810.4:c.*16G>T, NM_032810.4:c.*16G>A, NM_032810.3:c.*16G>T, NM_032810.3:c.*16G>A, NM_032810.2:c.*16G>T, NM_032810.2:c.*16G>A, XM_017016847.3:c.*16G>T, XM_017016847.3:c.*16G>A, XM_017016847.2:c.*16G>T, XM_017016847.2:c.*16G>A, XM_017016847.1:c.*16G>T, XM_017016847.1:c.*16G>A, XM_017016848.2:c.*16G>T, XM_017016848.2:c.*16G>A, XM_017016848.1:c.*16G>T, XM_017016848.1:c.*16G>A, NM_001321969.2:c.*16G>T, NM_001321969.2:c.*16G>A, NM_001321969.1:c.*16G>T, NM_001321969.1:c.*16G>A, NR_135914.2:n.1262G>T, NR_135914.2:n.1262G>A, NR_135914.1:n.1267G>T, NR_135914.1:n.1267G>A, NM_001321967.2:c.*16G>T, NM_001321967.2:c.*16G>A, NM_001321967.1:c.*16G>T, NM_001321967.1:c.*16G>A, NM_001321968.2:c.*16G>T, NM_001321968.2:c.*16G>A, NM_001321968.1:c.*16G>T, NM_001321968.1:c.*16G>A, XM_011540302.2:c.*16G>T, XM_011540302.2:c.*16G>A, XM_011540302.1:c.*16G>T, XM_011540302.1:c.*16G>A, XM_047425908.1:c.*16G>T, XM_047425908.1:c.*16G>A

Select item 149091855615.

rs1490918556 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:87827786 (GRCh38)
10:89587543 (GRCh37)
Canonical SPDI:: NC_000010.11:87827785:G:A
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.87827786G>A, NC_000010.10:g.89587543G>A, NW_013171807.1:g.43608G>A

Select item 149090233716.

rs1490902337 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:87794917 (GRCh38)
10:89554674 (GRCh37)
Canonical SPDI:: NC_000010.11:87794916:T:C
Gene:: ATAD1 (Varview), LOC124902476 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.87794917T>C, NC_000010.10:g.89554674T>C, NW_013171807.1:g.10739T>C

Select item 149088176417.

rs1490881764 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:87838306 (GRCh38)
10:89598063 (GRCh37)
Canonical SPDI:: NC_000010.11:87838305:C:T
Gene:: ATAD1 (Varview), CFL1P1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000318/5 (TOMMO)
T=0.000546/1 (Korea1K)
T=0.001027/3 (KOREAN)
HGVS:: NC_000010.11:g.87838306C>T, NC_000010.10:g.89598063C>T, NW_013171807.1:g.54128C>T

Select item 149087317618.

rs1490873176 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:87780319 (GRCh38)
10:89540076 (GRCh37)
Canonical SPDI:: NC_000010.11:87780318:G:A
Gene:: ATAD1 (Varview), LOC124902476 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.87780319G>A, NC_000010.10:g.89540076G>A

Select item 149086688519.

rs1490866885 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:87767697 (GRCh38)
10:89527454 (GRCh37)
Canonical SPDI:: NC_000010.11:87767696:C:T
Gene:: ATAD1 (Varview), LOC124902476 (Varview)
Functional Consequence:: synonymous_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant
HGVS:: NC_000010.11:g.87767697C>T, NC_000010.10:g.89527454C>T, XM_005270252.6:c.807G>A, XM_005270252.5:c.807G>A, XM_005270252.4:c.807G>A, XM_005270252.3:c.807G>A, XM_005270252.2:c.807G>A, XM_005270252.1:c.807G>A, NM_032810.4:c.807G>A, NM_032810.3:c.807G>A, NM_032810.2:c.807G>A, XM_011540303.4:c.807G>A, XM_011540303.3:c.807G>A, XM_011540303.2:c.807G>A, XM_011540303.1:c.807G>A, XM_017016847.3:c.807G>A, XM_017016847.2:c.807G>A, XM_017016847.1:c.807G>A, XM_017016848.2:c.717G>A, XM_017016848.1:c.717G>A, NM_001321969.2:c.450G>A, NM_001321969.1:c.450G>A, NR_135914.2:n.880G>A, NR_135914.1:n.885G>A, NM_001321967.2:c.807G>A, NM_001321967.1:c.807G>A, NM_001321968.2:c.717G>A, NM_001321968.1:c.717G>A, XM_011540302.2:c.633G>A, XM_011540302.1:c.633G>A, XR_007062224.1:n.20C>T, XM_047425908.1:c.807G>A, XM_047425910.1:c.807G>A, XM_047425911.1:c.807G>A, XM_047425912.1:c.807G>A, XM_047425913.1:c.717G>A

Select item 149078396620.

rs1490783966 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:87763819 (GRCh38)
10:89523576 (GRCh37)
Canonical SPDI:: NC_000010.11:87763818:G:A
Gene:: ATAD1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.87763819G>A, NC_000010.10:g.89523576G>A

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