SNP Links for Gene (Select 65991) - SNP

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Items: 1 to 20 of 4596

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Select item 14908903721.

rs1490890372 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:155056581 (GRCh38)
X:154284856 (GRCh37)
Canonical SPDI:: NC_000023.11:155056580:T:C
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.155056581T>C, NW_003871103.3:g.2490560T>C, NC_000023.10:g.154284856T>C, NM_023934.4:c.*1909T>C, NM_023934.3:c.*1909T>C

Select item 14908590912.

rs1490859091 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:155056030 (GRCh38)
X:154284305 (GRCh37)
Canonical SPDI:: NC_000023.11:155056029:A:G
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.155056030A>G, NW_003871103.3:g.2490009A>G, NC_000023.10:g.154284305A>G, NM_023934.4:c.*1358A>G, NM_023934.3:c.*1358A>G

Select item 14907876423.

rs1490787642 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:155045387 (GRCh38)
X:154273662 (GRCh37)
Canonical SPDI:: NC_000023.11:155045386:G:A
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.155045387G>A, NW_003871103.3:g.2479366G>A, NC_000023.10:g.154273662G>A

Select item 14907519804.

rs1490751980 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAT>- [Show Flanks]
Chromosome:: X:155043464 (GRCh38)
X:154271739 (GRCh37)
Canonical SPDI:: NC_000023.11:155043460:TATTAT:TAT
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TATTAT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.155043461TAT[1], NW_003871103.3:g.2477440TAT[1], NC_000023.10:g.154271736TAT[1]

Select item 14906584845.

rs1490658484 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:155032363 (GRCh38)
X:154260638 (GRCh37)
Canonical SPDI:: NC_000023.11:155032362:C:T
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00005/5 (GnomAD)
HGVS:: NC_000023.11:g.155032363C>T, NW_003871103.3:g.2466342C>T, NC_000023.10:g.154260638C>T

Select item 14904001366.

rs1490400136 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:155056917 (GRCh38)
X:154285192 (GRCh37)
Canonical SPDI:: NC_000023.11:155056916:G:A
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.155056917G>A, NW_003871103.3:g.2490896G>A, NC_000023.10:g.154285192G>A, NM_023934.4:c.*2245G>A

Select item 14903693917.

rs1490369391 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:155056308 (GRCh38)
X:154284583 (GRCh37)
Canonical SPDI:: NC_000023.11:155056307:G:T
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000023.11:g.155056308G>T, NW_003871103.3:g.2490287G>T, NC_000023.10:g.154284583G>T, NM_023934.4:c.*1636G>T, NM_023934.3:c.*1636G>T

Select item 14903303558.

rs1490330355 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:155031169 (GRCh38)
X:154259444 (GRCh37)
Canonical SPDI:: NC_000023.11:155031168:A:G
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000142/2 (ALFA)
G=0.000029/3 (GnomAD)
G=0.000038/10 (TOPMED)
HGVS:: NC_000023.11:g.155031169A>G, NW_003871103.3:g.2465148A>G, NC_000023.10:g.154259444A>G

Select item 14900965529.

rs1490096552 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTT [Show Flanks]
Chromosome:: X:155056318 (GRCh38)
X:154284594 (GRCh37)
Canonical SPDI:: NC_000023.11:155056318:T:TTTT
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
TTT=0.000042/11 (TOPMED)
TTT=0.000048/5 (GnomAD)
HGVS:: NC_000023.11:g.155056319_155056320insTTT, NW_003871103.3:g.2490298_2490299insTTT, NC_000023.10:g.154284594_154284595insTTT, NM_023934.4:c.*1647_*1648insTTT, NM_023934.3:c.*1647_*1648insTTT

Select item 149004226610.

rs1490042266 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GC [Show Flanks]
Chromosome:: X:155055628 (GRCh38)
X:154283904 (GRCh37)
Canonical SPDI:: NC_000023.11:155055628:C:CGC
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CGC=0./0 (ALFA)
CG=0.00001/1 (GnomAD)
CG=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.155055629_155055630insGC, NW_003871103.3:g.2489608_2489609insGC, NC_000023.10:g.154283904_154283905insGC, NM_023934.4:c.*957_*958insGC, NM_023934.3:c.*957_*958insGC

Select item 148996863411.

rs1489968634 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:155044626 (GRCh38)
X:154272901 (GRCh37)
Canonical SPDI:: NC_000023.11:155044625:A:G
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.155044626A>G, NW_003871103.3:g.2478605A>G, NC_000023.10:g.154272901A>G

Select item 148993355712.

rs1489933557 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:155042551 (GRCh38)
X:154270826 (GRCh37)
Canonical SPDI:: NC_000023.11:155042550:A:G
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.155042551A>G, NW_003871103.3:g.2476530A>G, NC_000023.10:g.154270826A>G

Select item 148984010613.

rs1489840106 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:155031952 (GRCh38)
X:154260227 (GRCh37)
Canonical SPDI:: NC_000023.11:155031951:A:G
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.155031952A>G, NW_003871103.3:g.2465931A>G, NC_000023.10:g.154260227A>G

Select item 148982451714.

rs1489824517 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:155030365 (GRCh38)
X:154258640 (GRCh37)
Canonical SPDI:: NC_000023.11:155030364:T:A
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.04408/128 (KOREAN)
HGVS:: NC_000023.11:g.155030365T>A, NW_003871103.3:g.2464344T>A, NC_000023.10:g.154258640T>A

Select item 148929045815.

rs1489290458 has merged into rs200182765 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTCT>- [Show Flanks]
Chromosome:: X:155040960 (GRCh38)
X:154269235 (GRCh37)
Canonical SPDI:: NC_000023.11:155040958:TGTCT:T
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.009466/133 (ALFA)
-=0.00027/1 (TWINSUK)
-=0.000346/1 (ALSPAC)
-=0.00531/68 (TOMMO)
-=0.013844/1445 (GnomAD)
-=0.026223/99 (1000Genomes)
-=0.027368/7244 (TOPMED)
HGVS:: NC_000023.11:g.155040960_155040963del, NW_003871103.3:g.2474939_2474942del, NC_000023.10:g.154269235_154269238del

Select item 148912249216.

rs1489122492 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: X:155055515 (GRCh38)
X:154283790 (GRCh37)
Canonical SPDI:: NC_000023.11:155055514:G:C,NC_000023.11:155055514:G:T
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.155055515G>C, NC_000023.11:g.155055515G>T, NW_003871103.3:g.2489494G>C, NW_003871103.3:g.2489494G>T, NC_000023.10:g.154283790G>C, NC_000023.10:g.154283790G>T, NM_023934.4:c.*843G>C, NM_023934.4:c.*843G>T, NM_023934.3:c.*843G>C, NM_023934.3:c.*843G>T

Select item 148903772717.

rs1489037727 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:155057169 (GRCh38)
X:154285444 (GRCh37)
Canonical SPDI:: NC_000023.11:155057168:C:G
Gene:: FUNDC2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.155057169C>G, NW_003871103.3:g.2491148C>G, NC_000023.10:g.154285444C>G, NM_023934.4:c.*2497C>G

Select item 148902841518.

rs1489028415 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:155053988 (GRCh38)
X:154282263 (GRCh37)
Canonical SPDI:: NC_000023.11:155053987:A:C
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.155053988A>C, NW_003871103.3:g.2487967A>C, NC_000023.10:g.154282263A>C

Select item 148901835019.

rs1489018350 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:155035820 (GRCh38)
X:154264095 (GRCh37)
Canonical SPDI:: NC_000023.11:155035819:C:T
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.155035820C>T, NW_003871103.3:g.2469799C>T, NC_000023.10:g.154264095C>T

Select item 148894770020.

rs1488947700 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:155034100 (GRCh38)
X:154262375 (GRCh37)
Canonical SPDI:: NC_000023.11:155034099:G:C
Gene:: FUNDC2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.155034100G>C, NW_003871103.3:g.2468079G>C, NC_000023.10:g.154262375G>C

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