SNP Links for Gene (Select 158809) - SNP

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Select item 14908709321.

rs1490870932 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:26193032 (GRCh38)
X:26211149 (GRCh37)
Canonical SPDI:: NC_000023.11:26193031:A:G
Gene:: MAGEB6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
G=0.000058/6 (GnomAD)
HGVS:: NC_000023.11:g.26193032A>G, NC_000023.10:g.26211149A>G, NG_013247.1:g.5593A>G

Select item 14895873022.

rs1489587302 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:26195235 (GRCh38)
X:26213352 (GRCh37)
Canonical SPDI:: NC_000023.11:26195234:A:C
Gene:: MAGEB6 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency
MAF:: C=0.00002/1 (GnomAD)
HGVS:: NC_000023.11:g.26195235A>C, NC_000023.10:g.26213352A>C, NG_013247.1:g.7796A>C, NM_173523.2:c.*165A>C

Select item 14892109643.

rs1489210964 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:26192413 (GRCh38)
X:26210530 (GRCh37)
Canonical SPDI:: NC_000023.11:26192412:G:A
Gene:: MAGEB6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.26192413G>A, NC_000023.10:g.26210530G>A, NG_013247.1:g.4974G>A

Select item 14890961814.

rs1489096181 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:26193612 (GRCh38)
X:26211729 (GRCh37)
Canonical SPDI:: NC_000023.11:26193611:T:C
Gene:: MAGEB6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/2 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.26193612T>C, NC_000023.10:g.26211729T>C, NG_013247.1:g.6173T>C

Select item 14878652875.

rs1487865287 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:26195138 (GRCh38)
X:26213255 (GRCh37)
Canonical SPDI:: NC_000023.11:26195137:T:A
Gene:: MAGEB6 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.26195138T>A, NC_000023.10:g.26213255T>A, NG_013247.1:g.7699T>A, NM_173523.2:c.*68T>A

Select item 14877535646.

rs1487753564 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:26192636 (GRCh38)
X:26210753 (GRCh37)
Canonical SPDI:: NC_000023.11:26192635:C:A,NC_000023.11:26192635:C:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.26192636C>A, NC_000023.11:g.26192636C>T, NC_000023.10:g.26210753C>A, NC_000023.10:g.26210753C>T, NG_013247.1:g.5197C>A, NG_013247.1:g.5197C>T

Select item 14859712477.

rs1485971247 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:26190640 (GRCh38)
X:26208757 (GRCh37)
Canonical SPDI:: NC_000023.11:26190639:A:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.26190640A>T, NC_000023.10:g.26208757A>T, NG_013247.1:g.3201A>T

Select item 14859410488.

rs1485941048 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:26192163 (GRCh38)
X:26210280 (GRCh37)
Canonical SPDI:: NC_000023.11:26192162:T:C
Gene:: MAGEB6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.26192163T>C, NC_000023.10:g.26210280T>C, NG_013247.1:g.4724T>C

Select item 14858596679.

rs1485859667 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: X:26192447 (GRCh38)
X:26210564 (GRCh37)
Canonical SPDI:: NC_000023.11:26192446:G:A,NC_000023.11:26192446:G:C
Gene:: MAGEB6 (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (KOREAN)
C=0.000091/24 (TOPMED)
C=0.000315/4 (TOMMO)
C=0.020833/1 (Vietnamese)
HGVS:: NC_000023.11:g.26192447G>A, NC_000023.11:g.26192447G>C, NC_000023.10:g.26210564G>A, NC_000023.10:g.26210564G>C, NG_013247.1:g.5008G>A, NG_013247.1:g.5008G>C, NM_173523.2:c.-142G>A, NM_173523.2:c.-142G>C

Select item 148287235810.

rs1482872358 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: X:26190773 (GRCh38)
X:26208890 (GRCh37)
Canonical SPDI:: NC_000023.11:26190772:A:G,NC_000023.11:26190772:A:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.26190773A>G, NC_000023.11:g.26190773A>T, NC_000023.10:g.26208890A>G, NC_000023.10:g.26208890A>T, NG_013247.1:g.3334A>G, NG_013247.1:g.3334A>T

Select item 148284293311.

rs1482842933 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: X:26192297 (GRCh38)
X:26210415 (GRCh37)
Canonical SPDI:: NC_000023.11:26192297:CCCC:CCCCC
Gene:: MAGEB6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CCCCC=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.26192301dup, NC_000023.10:g.26210418dup, NG_013247.1:g.4862dup

Select item 148235831412.

rs1482358314 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:26194739 (GRCh38)
X:26212856 (GRCh37)
Canonical SPDI:: NC_000023.11:26194738:A:G
Gene:: MAGEB6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000065/12 (GnomAD_exomes)
HGVS:: NC_000023.11:g.26194739A>G, NC_000023.10:g.26212856A>G, NG_013247.1:g.7300A>G, NM_173523.2:c.893A>G, NP_775794.2:p.Asn298Ser

Select item 148157215713.

rs1481572157 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:26192667 (GRCh38)
X:26210784 (GRCh37)
Canonical SPDI:: NC_000023.11:26192666:C:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.001566/7 (ALFA)
T=0.000058/6 (GnomAD)
HGVS:: NC_000023.11:g.26192667C>T, NC_000023.10:g.26210784C>T, NG_013247.1:g.5228C>T

Select item 148104157514.

rs1481041575 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:26193065 (GRCh38)
X:26211182 (GRCh37)
Canonical SPDI:: NC_000023.11:26193064:C:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000023.11:g.26193065C>T, NC_000023.10:g.26211182C>T, NG_013247.1:g.5626C>T

Select item 148071141515.

rs1480711415 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:26191141 (GRCh38)
X:26209258 (GRCh37)
Canonical SPDI:: NC_000023.11:26191140:C:A
Gene:: MAGEB6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.26191141C>A, NC_000023.10:g.26209258C>A, NG_013247.1:g.3702C>A

Select item 148040291116.

rs1480402911 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:26193888 (GRCh38)
X:26212005 (GRCh37)
Canonical SPDI:: NC_000023.11:26193887:A:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.26193888A>T, NC_000023.10:g.26212005A>T, NG_013247.1:g.6449A>T, NM_173523.2:c.42A>T, NP_775794.2:p.Lys14Asn

Select item 147975118717.

rs1479751187 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:26194854 (GRCh38)
X:26212971 (GRCh37)
Canonical SPDI:: NC_000023.11:26194853:G:A
Gene:: MAGEB6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.26194854G>A, NC_000023.10:g.26212971G>A, NG_013247.1:g.7415G>A, NM_173523.2:c.1008G>A

Select item 147936123818.

rs1479361238 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:26195346 (GRCh38)
X:26213463 (GRCh37)
Canonical SPDI:: NC_000023.11:26195345:A:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000077/8 (GnomAD)
T=0.000087/23 (TOPMED)
HGVS:: NC_000023.11:g.26195346A>T, NC_000023.10:g.26213463A>T, NG_013247.1:g.7907A>T, NM_173523.2:c.*276A>T

Select item 147835746019.

rs1478357460 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:26194521 (GRCh38)
X:26212638 (GRCh37)
Canonical SPDI:: NC_000023.11:26194520:C:T
Gene:: MAGEB6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.26194521C>T, NC_000023.10:g.26212638C>T, NG_013247.1:g.7082C>T, NM_173523.2:c.675C>T

Select item 147742677320.

rs1477426773 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:26191095 (GRCh38)
X:26209212 (GRCh37)
Canonical SPDI:: NC_000023.11:26191094:T:C
Gene:: MAGEB6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000023.11:g.26191095T>C, NC_000023.10:g.26209212T>C, NG_013247.1:g.3656T>C

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