SNP Links for Gene (Select 25780) - SNP

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Select item 14915865281.

rs1491586528 has merged into rs775598057 [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 [Show Flanks]
Chromosome:: 2:33548370 (GRCh38)
2:33773437 (GRCh37)
Canonical SPDI:: NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33548360:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.175/7 (GENOME_DK)
HGVS:: NC_000002.12:g.33548370_33548383del, NC_000002.12:g.33548371_33548383del, NC_000002.12:g.33548372_33548383del, NC_000002.12:g.33548373_33548383del, NC_000002.12:g.33548374_33548383del, NC_000002.12:g.33548375_33548383del, NC_000002.12:g.33548376_33548383del, NC_000002.12:g.33548377_33548383del, NC_000002.12:g.33548378_33548383del, NC_000002.12:g.33548379_33548383del, NC_000002.12:g.33548380_33548383del, NC_000002.12:g.33548381_33548383del, NC_000002.12:g.33548382_33548383del, NC_000002.12:g.33548383del, NC_000002.12:g.33548383dup, NC_000002.12:g.33548382_33548383dup, NC_000002.12:g.33548381_33548383dup, NC_000002.12:g.33548380_33548383dup, NC_000002.12:g.33548379_33548383dup, NC_000002.12:g.33548378_33548383dup, NC_000002.12:g.33548377_33548383dup, NC_000002.11:g.33773437_33773450del, NC_000002.11:g.33773438_33773450del, NC_000002.11:g.33773439_33773450del, NC_000002.11:g.33773440_33773450del, NC_000002.11:g.33773441_33773450del, NC_000002.11:g.33773442_33773450del, NC_000002.11:g.33773443_33773450del, NC_000002.11:g.33773444_33773450del, NC_000002.11:g.33773445_33773450del, NC_000002.11:g.33773446_33773450del, NC_000002.11:g.33773447_33773450del, NC_000002.11:g.33773448_33773450del, NC_000002.11:g.33773449_33773450del, NC_000002.11:g.33773450del, NC_000002.11:g.33773450dup, NC_000002.11:g.33773449_33773450dup, NC_000002.11:g.33773448_33773450dup, NC_000002.11:g.33773447_33773450dup, NC_000002.11:g.33773446_33773450dup, NC_000002.11:g.33773445_33773450dup, NC_000002.11:g.33773444_33773450dup, NG_053077.1:g.117023_117036del, NG_053077.1:g.117024_117036del, NG_053077.1:g.117025_117036del, NG_053077.1:g.117026_117036del, NG_053077.1:g.117027_117036del, NG_053077.1:g.117028_117036del, NG_053077.1:g.117029_117036del, NG_053077.1:g.117030_117036del, NG_053077.1:g.117031_117036del, NG_053077.1:g.117032_117036del, NG_053077.1:g.117033_117036del, NG_053077.1:g.117034_117036del, NG_053077.1:g.117035_117036del, NG_053077.1:g.117036del, NG_053077.1:g.117036dup, NG_053077.1:g.117035_117036dup, NG_053077.1:g.117034_117036dup, NG_053077.1:g.117033_117036dup, NG_053077.1:g.117032_117036dup, NG_053077.1:g.117031_117036dup, NG_053077.1:g.117030_117036dup

Select item 14915816472.

rs1491581647 has merged into rs767124838 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 2:33547063 (GRCh38)
2:33772130 (GRCh37)
Canonical SPDI:: NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:33547053:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000002.12:g.33547063_33547074del, NC_000002.12:g.33547064_33547074del, NC_000002.12:g.33547065_33547074del, NC_000002.12:g.33547066_33547074del, NC_000002.12:g.33547067_33547074del, NC_000002.12:g.33547068_33547074del, NC_000002.12:g.33547069_33547074del, NC_000002.12:g.33547070_33547074del, NC_000002.12:g.33547071_33547074del, NC_000002.12:g.33547072_33547074del, NC_000002.12:g.33547073_33547074del, NC_000002.12:g.33547074del, NC_000002.12:g.33547074dup, NC_000002.12:g.33547073_33547074dup, NC_000002.12:g.33547072_33547074dup, NC_000002.12:g.33547071_33547074dup, NC_000002.12:g.33547070_33547074dup, NC_000002.12:g.33547068_33547074dup, NC_000002.12:g.33547074_33547075insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000002.12:g.33547054_33547074A[22]GAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000002.11:g.33772130_33772141del, NC_000002.11:g.33772131_33772141del, NC_000002.11:g.33772132_33772141del, NC_000002.11:g.33772133_33772141del, NC_000002.11:g.33772134_33772141del, NC_000002.11:g.33772135_33772141del, NC_000002.11:g.33772136_33772141del, NC_000002.11:g.33772137_33772141del, NC_000002.11:g.33772138_33772141del, NC_000002.11:g.33772139_33772141del, NC_000002.11:g.33772140_33772141del, NC_000002.11:g.33772141del, NC_000002.11:g.33772141dup, NC_000002.11:g.33772140_33772141dup, NC_000002.11:g.33772139_33772141dup, NC_000002.11:g.33772138_33772141dup, NC_000002.11:g.33772137_33772141dup, NC_000002.11:g.33772135_33772141dup, NC_000002.11:g.33772141_33772142insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000002.11:g.33772121_33772141A[22]GAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_053077.1:g.115716_115727del, NG_053077.1:g.115717_115727del, NG_053077.1:g.115718_115727del, NG_053077.1:g.115719_115727del, NG_053077.1:g.115720_115727del, NG_053077.1:g.115721_115727del, NG_053077.1:g.115722_115727del, NG_053077.1:g.115723_115727del, NG_053077.1:g.115724_115727del, NG_053077.1:g.115725_115727del, NG_053077.1:g.115726_115727del, NG_053077.1:g.115727del, NG_053077.1:g.115727dup, NG_053077.1:g.115726_115727dup, NG_053077.1:g.115725_115727dup, NG_053077.1:g.115724_115727dup, NG_053077.1:g.115723_115727dup, NG_053077.1:g.115721_115727dup, NG_053077.1:g.115727_115728insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_053077.1:g.115707_115727A[22]GAAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 14915736363.

rs1491573636 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 2:33548360 (GRCh38)
2:33773427 (GRCh37)
Canonical SPDI:: NC_000002.12:33548359:CA:
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01399/166 (ALFA)
-=0.00118/2 (Korea1K)
-=0.00354/57 (TOMMO)
HGVS:: NC_000002.12:g.33548360_33548361del, NC_000002.11:g.33773427_33773428del, NG_053077.1:g.117013_117014del

Select item 14915478484.

rs1491547848 [Homo sapiens]

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

Select item 14915442935.

rs1491544293 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 2:33470380 (GRCh38)
2:33695447 (GRCh37)
Canonical SPDI:: NC_000002.12:33470379:AT:
Gene:: RASGRP3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000002.12:g.33470380_33470381del, NC_000002.11:g.33695447_33695448del, NG_053077.1:g.39033_39034del

Select item 14915163426.

rs1491516342 has merged into rs377215232 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 2:33540576 (GRCh38)
2:33765643 (GRCh37)
Canonical SPDI:: NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000002.12:33540556:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
TGTGTGTGTGTG=0.000004/1 (TOPMED)
-=0.15/6 (GENOME_DK)
TGTG=0.25/2 (KOREAN)
HGVS:: NC_000002.12:g.33540558GT[9], NC_000002.12:g.33540558GT[10], NC_000002.12:g.33540558GT[11], NC_000002.12:g.33540558GT[13], NC_000002.12:g.33540558GT[14], NC_000002.12:g.33540558GT[15], NC_000002.12:g.33540558GT[16], NC_000002.12:g.33540558GT[17], NC_000002.12:g.33540558GT[18], NC_000002.12:g.33540558GT[19], NC_000002.12:g.33540558GT[20], NC_000002.12:g.33540558GT[21], NC_000002.12:g.33540558GT[22], NC_000002.12:g.33540558GT[23], NC_000002.12:g.33540558GT[25], NC_000002.12:g.33540558GT[26], NC_000002.12:g.33540558GT[27], NC_000002.12:g.33540558GT[28], NC_000002.12:g.33540558GT[29], NC_000002.12:g.33540558GT[30], NC_000002.12:g.33540558GT[31], NC_000002.12:g.33540558GT[32], NC_000002.11:g.33765625GT[9], NC_000002.11:g.33765625GT[10], NC_000002.11:g.33765625GT[11], NC_000002.11:g.33765625GT[13], NC_000002.11:g.33765625GT[14], NC_000002.11:g.33765625GT[15], NC_000002.11:g.33765625GT[16], NC_000002.11:g.33765625GT[17], NC_000002.11:g.33765625GT[18], NC_000002.11:g.33765625GT[19], NC_000002.11:g.33765625GT[20], NC_000002.11:g.33765625GT[21], NC_000002.11:g.33765625GT[22], NC_000002.11:g.33765625GT[23], NC_000002.11:g.33765625GT[25], NC_000002.11:g.33765625GT[26], NC_000002.11:g.33765625GT[27], NC_000002.11:g.33765625GT[28], NC_000002.11:g.33765625GT[29], NC_000002.11:g.33765625GT[30], NC_000002.11:g.33765625GT[31], NC_000002.11:g.33765625GT[32], NG_053077.1:g.109211GT[9], NG_053077.1:g.109211GT[10], NG_053077.1:g.109211GT[11], NG_053077.1:g.109211GT[13], NG_053077.1:g.109211GT[14], NG_053077.1:g.109211GT[15], NG_053077.1:g.109211GT[16], NG_053077.1:g.109211GT[17], NG_053077.1:g.109211GT[18], NG_053077.1:g.109211GT[19], NG_053077.1:g.109211GT[20], NG_053077.1:g.109211GT[21], NG_053077.1:g.109211GT[22], NG_053077.1:g.109211GT[23], NG_053077.1:g.109211GT[25], NG_053077.1:g.109211GT[26], NG_053077.1:g.109211GT[27], NG_053077.1:g.109211GT[28], NG_053077.1:g.109211GT[29], NG_053077.1:g.109211GT[30], NG_053077.1:g.109211GT[31], NG_053077.1:g.109211GT[32]

Select item 14915057107.

rs1491505710 [Homo sapiens]

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

Select item 14914978418.

rs1491497841 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 2:33486178 (GRCh38)
2:33711245 (GRCh37)
Canonical SPDI:: NC_000002.12:33486177:TG:
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000002.12:g.33486178_33486179del, NC_000002.11:g.33711245_33711246del, NG_053077.1:g.54831_54832del

Select item 14914963799.

rs1491496379 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TCTTT [Show Flanks]
Chromosome:: 2:33467979 (GRCh38)
2:33693047 (GRCh37)
Canonical SPDI:: NC_000002.12:33467979:TTTTCTTT:TTTTCTTTTCTTT
Gene:: RASGRP3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTCTTTTCTTT=0./0 (ALFA)
TTTTC=0.000049/5 (GnomAD)
HGVS:: NC_000002.12:g.33467983_33467987dup, NC_000002.11:g.33693050_33693054dup, NG_053077.1:g.36636_36640dup

Select item 149146131510.

rs1491461315 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT [Show Flanks]
Chromosome:: 2:33540554 (GRCh38)
2:33765622 (GRCh37)
Canonical SPDI:: NC_000002.12:33540554:T:TGT,NC_000002.12:33540554:T:TGTGT,NC_000002.12:33540554:T:TGTGTGT,NC_000002.12:33540554:T:TGTGTGTGT,NC_000002.12:33540554:T:TGTGTGTGTGT
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGT=0./0 (ALFA)
GT=0.00189/7 (TWINSUK)
GT=0.00415/16 (ALSPAC)
HGVS:: NC_000002.12:g.33540555_33540556insGT, NC_000002.12:g.33540555_33540556insGTGT, NC_000002.12:g.33540556GT[3], NC_000002.12:g.33540556GT[4], NC_000002.12:g.33540556GT[5], NC_000002.11:g.33765622_33765623insGT, NC_000002.11:g.33765622_33765623insGTGT, NC_000002.11:g.33765623GT[3], NC_000002.11:g.33765623GT[4], NC_000002.11:g.33765623GT[5], NG_053077.1:g.109208_109209insGT, NG_053077.1:g.109208_109209insGTGT, NG_053077.1:g.109209GT[3], NG_053077.1:g.109209GT[4], NG_053077.1:g.109209GT[5]

Select item 149145047011.

rs1491450470 has merged into rs59601670 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:33547353 (GRCh38)
2:33772420 (GRCh37)
Canonical SPDI:: NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33547342:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
TTTTTTTT=0./0 (GENOME_DK)
HGVS:: NC_000002.12:g.33547353_33547371del, NC_000002.12:g.33547354_33547371del, NC_000002.12:g.33547355_33547371del, NC_000002.12:g.33547356_33547371del, NC_000002.12:g.33547357_33547371del, NC_000002.12:g.33547358_33547371del, NC_000002.12:g.33547359_33547371del, NC_000002.12:g.33547360_33547371del, NC_000002.12:g.33547361_33547371del, NC_000002.12:g.33547362_33547371del, NC_000002.12:g.33547363_33547371del, NC_000002.12:g.33547364_33547371del, NC_000002.12:g.33547365_33547371del, NC_000002.12:g.33547366_33547371del, NC_000002.12:g.33547367_33547371del, NC_000002.12:g.33547368_33547371del, NC_000002.12:g.33547369_33547371del, NC_000002.12:g.33547370_33547371del, NC_000002.12:g.33547371del, NC_000002.12:g.33547371dup, NC_000002.12:g.33547370_33547371dup, NC_000002.12:g.33547369_33547371dup, NC_000002.12:g.33547368_33547371dup, NC_000002.12:g.33547367_33547371dup, NC_000002.12:g.33547366_33547371dup, NC_000002.12:g.33547365_33547371dup, NC_000002.12:g.33547364_33547371dup, NC_000002.12:g.33547363_33547371dup, NC_000002.12:g.33547362_33547371dup, NC_000002.12:g.33547361_33547371dup, NC_000002.12:g.33547360_33547371dup, NC_000002.12:g.33547359_33547371dup, NC_000002.12:g.33547358_33547371dup, NC_000002.12:g.33547357_33547371dup, NC_000002.12:g.33547356_33547371dup, NC_000002.12:g.33547355_33547371dup, NC_000002.12:g.33547354_33547371dup, NC_000002.12:g.33547353_33547371dup, NC_000002.12:g.33547352_33547371dup, NC_000002.12:g.33547351_33547371dup, NC_000002.12:g.33547350_33547371dup, NC_000002.12:g.33547349_33547371dup, NC_000002.12:g.33547348_33547371dup, NC_000002.12:g.33547347_33547371dup, NC_000002.12:g.33547346_33547371dup, NC_000002.12:g.33547345_33547371dup, NC_000002.12:g.33547344_33547371dup, NC_000002.12:g.33547343_33547371dup, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33547371_33547372insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772420_33772438del, NC_000002.11:g.33772421_33772438del, NC_000002.11:g.33772422_33772438del, NC_000002.11:g.33772423_33772438del, NC_000002.11:g.33772424_33772438del, NC_000002.11:g.33772425_33772438del, NC_000002.11:g.33772426_33772438del, NC_000002.11:g.33772427_33772438del, NC_000002.11:g.33772428_33772438del, NC_000002.11:g.33772429_33772438del, NC_000002.11:g.33772430_33772438del, NC_000002.11:g.33772431_33772438del, NC_000002.11:g.33772432_33772438del, NC_000002.11:g.33772433_33772438del, NC_000002.11:g.33772434_33772438del, NC_000002.11:g.33772435_33772438del, NC_000002.11:g.33772436_33772438del, NC_000002.11:g.33772437_33772438del, NC_000002.11:g.33772438del, NC_000002.11:g.33772438dup, NC_000002.11:g.33772437_33772438dup, NC_000002.11:g.33772436_33772438dup, NC_000002.11:g.33772435_33772438dup, NC_000002.11:g.33772434_33772438dup, NC_000002.11:g.33772433_33772438dup, NC_000002.11:g.33772432_33772438dup, NC_000002.11:g.33772431_33772438dup, NC_000002.11:g.33772430_33772438dup, NC_000002.11:g.33772429_33772438dup, NC_000002.11:g.33772428_33772438dup, NC_000002.11:g.33772427_33772438dup, NC_000002.11:g.33772426_33772438dup, NC_000002.11:g.33772425_33772438dup, NC_000002.11:g.33772424_33772438dup, NC_000002.11:g.33772423_33772438dup, NC_000002.11:g.33772422_33772438dup, NC_000002.11:g.33772421_33772438dup, NC_000002.11:g.33772420_33772438dup, NC_000002.11:g.33772419_33772438dup, NC_000002.11:g.33772418_33772438dup, NC_000002.11:g.33772417_33772438dup, NC_000002.11:g.33772416_33772438dup, NC_000002.11:g.33772415_33772438dup, NC_000002.11:g.33772414_33772438dup, NC_000002.11:g.33772413_33772438dup, NC_000002.11:g.33772412_33772438dup, NC_000002.11:g.33772411_33772438dup, NC_000002.11:g.33772410_33772438dup, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33772438_33772439insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116006_116024del, NG_053077.1:g.116007_116024del, NG_053077.1:g.116008_116024del, NG_053077.1:g.116009_116024del, NG_053077.1:g.116010_116024del, NG_053077.1:g.116011_116024del, NG_053077.1:g.116012_116024del, NG_053077.1:g.116013_116024del, NG_053077.1:g.116014_116024del, NG_053077.1:g.116015_116024del, NG_053077.1:g.116016_116024del, NG_053077.1:g.116017_116024del, NG_053077.1:g.116018_116024del, NG_053077.1:g.116019_116024del, NG_053077.1:g.116020_116024del, NG_053077.1:g.116021_116024del, NG_053077.1:g.116022_116024del, NG_053077.1:g.116023_116024del, NG_053077.1:g.116024del, NG_053077.1:g.116024dup, NG_053077.1:g.116023_116024dup, NG_053077.1:g.116022_116024dup, NG_053077.1:g.116021_116024dup, NG_053077.1:g.116020_116024dup, NG_053077.1:g.116019_116024dup, NG_053077.1:g.116018_116024dup, NG_053077.1:g.116017_116024dup, NG_053077.1:g.116016_116024dup, NG_053077.1:g.116015_116024dup, NG_053077.1:g.116014_116024dup, NG_053077.1:g.116013_116024dup, NG_053077.1:g.116012_116024dup, NG_053077.1:g.116011_116024dup, NG_053077.1:g.116010_116024dup, NG_053077.1:g.116009_116024dup, NG_053077.1:g.116008_116024dup, NG_053077.1:g.116007_116024dup, NG_053077.1:g.116006_116024dup, NG_053077.1:g.116005_116024dup, NG_053077.1:g.116004_116024dup, NG_053077.1:g.116003_116024dup, NG_053077.1:g.116002_116024dup, NG_053077.1:g.116001_116024dup, NG_053077.1:g.116000_116024dup, NG_053077.1:g.115999_116024dup, NG_053077.1:g.115998_116024dup, NG_053077.1:g.115997_116024dup, NG_053077.1:g.115996_116024dup, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.116024_116025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149144030012.

rs1491440300 has merged into rs560214980 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>-,AGAG [Show Flanks]
Chromosome:: 2:33486190 (GRCh38)
2:33711257 (GRCh37)
Canonical SPDI:: NC_000002.12:33486178:GAGAGAGAGAGAG:GAGAGAGAGAG,NC_000002.12:33486178:GAGAGAGAGAGAG:GAGAGAGAGAGAGAG
Gene:: RASGRP3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGAGAGAGAGAG=0./0 (ALFA)
GA=0.000336/37 (GnomAD)
-=0.0004/2 (1000Genomes)
-=0.004367/8 (Korea1K)
GA=0.008139/136 (TOMMO)
HGVS:: NC_000002.12:g.33486180AG[5], NC_000002.12:g.33486180AG[7], NC_000002.11:g.33711247AG[5], NC_000002.11:g.33711247AG[7], NG_053077.1:g.54833AG[5], NG_053077.1:g.54833AG[7]

Select item 149143612113.

rs1491436121 has merged into rs746592952 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:33530506 (GRCh38)
2:33755573 (GRCh37)
Canonical SPDI:: NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33530497:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
-=0.475/19 (GENOME_DK)
HGVS:: NC_000002.12:g.33530506_33530521del, NC_000002.12:g.33530507_33530521del, NC_000002.12:g.33530508_33530521del, NC_000002.12:g.33530509_33530521del, NC_000002.12:g.33530510_33530521del, NC_000002.12:g.33530511_33530521del, NC_000002.12:g.33530512_33530521del, NC_000002.12:g.33530514_33530521del, NC_000002.12:g.33530515_33530521del, NC_000002.12:g.33530516_33530521del, NC_000002.12:g.33530517_33530521del, NC_000002.12:g.33530518_33530521del, NC_000002.12:g.33530519_33530521del, NC_000002.12:g.33530520_33530521del, NC_000002.12:g.33530521del, NC_000002.12:g.33530521dup, NC_000002.12:g.33530520_33530521dup, NC_000002.12:g.33530519_33530521dup, NC_000002.12:g.33530518_33530521dup, NC_000002.12:g.33530517_33530521dup, NC_000002.12:g.33530516_33530521dup, NC_000002.12:g.33530512_33530521dup, NC_000002.12:g.33530510_33530521dup, NC_000002.12:g.33530509_33530521dup, NC_000002.11:g.33755573_33755588del, NC_000002.11:g.33755574_33755588del, NC_000002.11:g.33755575_33755588del, NC_000002.11:g.33755576_33755588del, NC_000002.11:g.33755577_33755588del, NC_000002.11:g.33755578_33755588del, NC_000002.11:g.33755579_33755588del, NC_000002.11:g.33755581_33755588del, NC_000002.11:g.33755582_33755588del, NC_000002.11:g.33755583_33755588del, NC_000002.11:g.33755584_33755588del, NC_000002.11:g.33755585_33755588del, NC_000002.11:g.33755586_33755588del, NC_000002.11:g.33755587_33755588del, NC_000002.11:g.33755588del, NC_000002.11:g.33755588dup, NC_000002.11:g.33755587_33755588dup, NC_000002.11:g.33755586_33755588dup, NC_000002.11:g.33755585_33755588dup, NC_000002.11:g.33755584_33755588dup, NC_000002.11:g.33755583_33755588dup, NC_000002.11:g.33755579_33755588dup, NC_000002.11:g.33755577_33755588dup, NC_000002.11:g.33755576_33755588dup, NG_053077.1:g.99159_99174del, NG_053077.1:g.99160_99174del, NG_053077.1:g.99161_99174del, NG_053077.1:g.99162_99174del, NG_053077.1:g.99163_99174del, NG_053077.1:g.99164_99174del, NG_053077.1:g.99165_99174del, NG_053077.1:g.99167_99174del, NG_053077.1:g.99168_99174del, NG_053077.1:g.99169_99174del, NG_053077.1:g.99170_99174del, NG_053077.1:g.99171_99174del, NG_053077.1:g.99172_99174del, NG_053077.1:g.99173_99174del, NG_053077.1:g.99174del, NG_053077.1:g.99174dup, NG_053077.1:g.99173_99174dup, NG_053077.1:g.99172_99174dup, NG_053077.1:g.99171_99174dup, NG_053077.1:g.99170_99174dup, NG_053077.1:g.99169_99174dup, NG_053077.1:g.99165_99174dup, NG_053077.1:g.99163_99174dup, NG_053077.1:g.99162_99174dup

Select item 149141836514.

rs1491418365 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 2:33471363 (GRCh38)
2:33696430 (GRCh37)
Canonical SPDI:: NC_000002.12:33471361:TGT:T
Gene:: RASGRP3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.33471363_33471364del, NC_000002.11:g.33696430_33696431del, NG_053077.1:g.40016_40017del

Select item 149140316715.

rs1491403167 has merged into rs202150682 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:33483497 (GRCh38)
2:33708564 (GRCh37)
Canonical SPDI:: NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:33483486:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.1999/1001 (1000Genomes)
HGVS:: NC_000002.12:g.33483497_33483506del, NC_000002.12:g.33483498_33483506del, NC_000002.12:g.33483499_33483506del, NC_000002.12:g.33483500_33483506del, NC_000002.12:g.33483501_33483506del, NC_000002.12:g.33483502_33483506del, NC_000002.12:g.33483503_33483506del, NC_000002.12:g.33483504_33483506del, NC_000002.12:g.33483505_33483506del, NC_000002.12:g.33483506del, NC_000002.12:g.33483506dup, NC_000002.12:g.33483505_33483506dup, NC_000002.12:g.33483504_33483506dup, NC_000002.12:g.33483503_33483506dup, NC_000002.12:g.33483502_33483506dup, NC_000002.12:g.33483501_33483506dup, NC_000002.12:g.33483500_33483506dup, NC_000002.12:g.33483499_33483506dup, NC_000002.12:g.33483506_33483507insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.12:g.33483506_33483507insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33708564_33708573del, NC_000002.11:g.33708565_33708573del, NC_000002.11:g.33708566_33708573del, NC_000002.11:g.33708567_33708573del, NC_000002.11:g.33708568_33708573del, NC_000002.11:g.33708569_33708573del, NC_000002.11:g.33708570_33708573del, NC_000002.11:g.33708571_33708573del, NC_000002.11:g.33708572_33708573del, NC_000002.11:g.33708573del, NC_000002.11:g.33708573dup, NC_000002.11:g.33708572_33708573dup, NC_000002.11:g.33708571_33708573dup, NC_000002.11:g.33708570_33708573dup, NC_000002.11:g.33708569_33708573dup, NC_000002.11:g.33708568_33708573dup, NC_000002.11:g.33708567_33708573dup, NC_000002.11:g.33708566_33708573dup, NC_000002.11:g.33708573_33708574insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.33708573_33708574insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.52150_52159del, NG_053077.1:g.52151_52159del, NG_053077.1:g.52152_52159del, NG_053077.1:g.52153_52159del, NG_053077.1:g.52154_52159del, NG_053077.1:g.52155_52159del, NG_053077.1:g.52156_52159del, NG_053077.1:g.52157_52159del, NG_053077.1:g.52158_52159del, NG_053077.1:g.52159del, NG_053077.1:g.52159dup, NG_053077.1:g.52158_52159dup, NG_053077.1:g.52157_52159dup, NG_053077.1:g.52156_52159dup, NG_053077.1:g.52155_52159dup, NG_053077.1:g.52154_52159dup, NG_053077.1:g.52153_52159dup, NG_053077.1:g.52152_52159dup, NG_053077.1:g.52159_52160insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_053077.1:g.52159_52160insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149136574016.

rs1491365740 [Homo sapiens]

Variant type:: INS
Alleles:: ->AT,ATT,ATTT [Show Flanks]
Chromosome:: 2:33530497 (GRCh38)
2:33755565 (GRCh37)
Canonical SPDI:: NC_000002.12:33530497::AT,NC_000002.12:33530497::ATT,NC_000002.12:33530497::ATTT
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATT=0./0 (ALFA)
HGVS:: NC_000002.12:g.33530497_33530498insAT, NC_000002.12:g.33530497_33530498insATT, NC_000002.12:g.33530497_33530498insATTT, NC_000002.11:g.33755564_33755565insAT, NC_000002.11:g.33755564_33755565insATT, NC_000002.11:g.33755564_33755565insATTT, NG_053077.1:g.99150_99151insAT, NG_053077.1:g.99150_99151insATT, NG_053077.1:g.99150_99151insATTT

Select item 149135968117.

rs1491359681 has merged into rs1270234762 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,TT,TTT,TTTTT [Show Flanks]
Chromosome:: 2:33467980 (GRCh38)
2:33693047 (GRCh37)
Canonical SPDI:: NC_000002.12:33467978:TTTTT:T,NC_000002.12:33467978:TTTTT:TTT,NC_000002.12:33467978:TTTTT:TTTT,NC_000002.12:33467978:TTTTT:TTTTTT
Gene:: RASGRP3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTT=0./0 (ALFA)
-=0.00028/5 (TOMMO)
HGVS:: NC_000002.12:g.33467980_33467983del, NC_000002.12:g.33467982_33467983del, NC_000002.12:g.33467983del, NC_000002.12:g.33467983dup, NC_000002.11:g.33693047_33693050del, NC_000002.11:g.33693049_33693050del, NC_000002.11:g.33693050del, NC_000002.11:g.33693050dup, NG_053077.1:g.36633_36636del, NG_053077.1:g.36635_36636del, NG_053077.1:g.36636del, NG_053077.1:g.36636dup

Select item 149135956618.

rs1491359566 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 2:33562268 (GRCh38)
2:33787336 (GRCh37)
Canonical SPDI:: NC_000002.12:33562268::C
Gene:: RASGRP3 (Varview), RASGRP3-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00051/6 (ALFA)
C=0.00018/5 (TOMMO)
C=0.0008/25 (GnomAD)
HGVS:: NC_000002.12:g.33562268_33562269insC, NC_000002.11:g.33787335_33787336insC, NG_053077.1:g.130921_130922insC

Select item 149133380519.

rs1491333805 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 2:33525341 (GRCh38)
2:33750408 (GRCh37)
Canonical SPDI:: NC_000002.12:33525340:AA:
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.33525341_33525342del, NC_000002.11:g.33750408_33750409del, NG_053077.1:g.93994_93995del

Select item 149132626720.

rs1491326267 has merged into rs1194020372 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGA>-,GA [Show Flanks]
Chromosome:: 2:33552028 (GRCh38)
2:33777095 (GRCh37)
Canonical SPDI:: NC_000002.12:33552026:AGAGA:A,NC_000002.12:33552026:AGAGA:AGA
Gene:: RASGRP3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGA=0./0 (ALFA)
-=0.0027/10 (TWINSUK)
-=0.00285/11 (ALSPAC)
HGVS:: NC_000002.12:g.33552028_33552031del, NC_000002.12:g.33552028GA[1], NC_000002.11:g.33777095_33777098del, NC_000002.11:g.33777095GA[1], NG_053077.1:g.120681_120684del, NG_053077.1:g.120681GA[1]

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