SNP Links for Protein (Select 683523959) - SNP

Links from Protein

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Select item 14880608181.

rs1488060818 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:43267842 (GRCh38)
19:43771994 (GRCh37)
Canonical SPDI:: NC_000019.10:43267841:G:A
Gene:: PSG9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.43267842G>A, NC_000019.9:g.43771994G>A, XM_005259075.5:c.372C>T, NM_002784.5:c.372C>T, NM_002784.4:c.372C>T, NM_002784.3:c.372C>T, XM_017027007.3:c.372C>T, XM_017027007.2:c.372C>T, XM_017027007.1:c.372C>T, NM_001301708.2:c.372C>T, NM_001301708.1:c.372C>T, NM_001301707.2:c.372C>T, NM_001301707.1:c.372C>T, NM_001301709.2:c.372C>T, NM_001301709.1:c.372C>T, NM_001411075.1:c.372C>T

Select item 14800444122.

rs1480044412 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:43258340 (GRCh38)
19:43762492 (GRCh37)
Canonical SPDI:: NC_000019.10:43258339:T:C
Gene:: PSG9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.000112/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.43258340T>C, NC_000019.9:g.43762492T>C, XM_005259075.5:c.826A>G, NM_002784.5:c.1105A>G, NM_002784.4:c.1105A>G, NM_002784.3:c.1105A>G, XM_017027007.3:c.1105A>G, XM_017027007.2:c.1105A>G, XM_017027007.1:c.1105A>G, NM_001301708.2:c.826A>G, NM_001301708.1:c.826A>G, NM_001301707.2:c.826A>G, NM_001301707.1:c.826A>G, NM_001301709.2:c.547A>G, NM_001301709.1:c.547A>G, NM_001411075.1:c.826A>G, XP_005259132.1:p.Asn276Asp, NP_002775.3:p.Asn369Asp, XP_016882496.1:p.Asn369Asp, NP_001288637.1:p.Asn276Asp, NP_001288636.1:p.Asn276Asp, NP_001288638.1:p.Asn183Asp

Select item 14759588413.

rs1475958841 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:43267859 (GRCh38)
19:43772011 (GRCh37)
Canonical SPDI:: NC_000019.10:43267858:T:A
Gene:: PSG9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000051/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.43267859T>A, NC_000019.9:g.43772011T>A, XM_005259075.5:c.355A>T, NM_002784.5:c.355A>T, NM_002784.4:c.355A>T, NM_002784.3:c.355A>T, XM_017027007.3:c.355A>T, XM_017027007.2:c.355A>T, XM_017027007.1:c.355A>T, NM_001301708.2:c.355A>T, NM_001301708.1:c.355A>T, NM_001301707.2:c.355A>T, NM_001301707.1:c.355A>T, NM_001301709.2:c.355A>T, NM_001301709.1:c.355A>T, NM_001411075.1:c.355A>T, XP_005259132.1:p.Thr119Ser, NP_002775.3:p.Thr119Ser, XP_016882496.1:p.Thr119Ser, NP_001288637.1:p.Thr119Ser, NP_001288636.1:p.Thr119Ser, NP_001288638.1:p.Thr119Ser

Select item 14726452454.

rs1472645245 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 19:43258264 (GRCh38)
19:43762416 (GRCh37)
Canonical SPDI:: NC_000019.10:43258263:C:
Gene:: PSG9 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.43258264del, NC_000019.9:g.43762416del, XM_005259075.5:c.902del, NM_002784.5:c.1181del, NM_002784.4:c.1181del, NM_002784.3:c.1181del, XM_017027007.3:c.1181del, XM_017027007.2:c.1181del, XM_017027007.1:c.1181del, NM_001301708.2:c.902del, NM_001301708.1:c.902del, NM_001301707.2:c.902del, NM_001301707.1:c.902del, NM_001301709.2:c.623del, NM_001301709.1:c.623del, NM_001411075.1:c.902del, XP_005259132.1:p.Cys301fs, NP_002775.3:p.Cys394fs, XP_016882496.1:p.Cys394fs, NP_001288637.1:p.Cys301fs, NP_001288636.1:p.Cys301fs, NP_001288638.1:p.Cys208fs

Select item 14708495435.

rs1470849543 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:43253630 (GRCh38)
19:43757782 (GRCh37)
Canonical SPDI:: NC_000019.10:43253629:G:A,NC_000019.10:43253629:G:T
Gene:: PSG9 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,downstream_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.43253630G>A, NC_000019.10:g.43253630G>T, NC_000019.9:g.43757782G>A, NC_000019.9:g.43757782G>T, NM_002784.5:c.1260C>T, NM_002784.5:c.1260C>A, NM_002784.4:c.1260C>T, NM_002784.4:c.1260C>A, NM_002784.3:c.1260C>T, NM_002784.3:c.1260C>A, NM_001301708.2:c.981C>T, NM_001301708.2:c.981C>A, NM_001301708.1:c.981C>T, NM_001301708.1:c.981C>A, NM_001301707.2:c.981C>T, NM_001301707.2:c.981C>A, NM_001301707.1:c.981C>T, NM_001301707.1:c.981C>A, NM_001301709.2:c.702C>T, NM_001301709.2:c.702C>A, NM_001301709.1:c.702C>T, NM_001301709.1:c.702C>A, NP_002775.3:p.Asp420Glu, NP_001288637.1:p.Asp327Glu, NP_001288636.1:p.Asp327Glu, NP_001288638.1:p.Asp234Glu

Select item 14680771256.

rs1468077125 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:43258304 (GRCh38)
19:43762456 (GRCh37)
Canonical SPDI:: NC_000019.10:43258303:T:C
Gene:: PSG9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.43258304T>C, NC_000019.9:g.43762456T>C, XM_005259075.5:c.862A>G, NM_002784.5:c.1141A>G, NM_002784.4:c.1141A>G, NM_002784.3:c.1141A>G, XM_017027007.3:c.1141A>G, XM_017027007.2:c.1141A>G, XM_017027007.1:c.1141A>G, NM_001301708.2:c.862A>G, NM_001301708.1:c.862A>G, NM_001301707.2:c.862A>G, NM_001301707.1:c.862A>G, NM_001301709.2:c.583A>G, NM_001301709.1:c.583A>G, NM_001411075.1:c.862A>G, XP_005259132.1:p.Ile288Val, NP_002775.3:p.Ile381Val, XP_016882496.1:p.Ile381Val, NP_001288637.1:p.Ile288Val, NP_001288636.1:p.Ile288Val, NP_001288638.1:p.Ile195Val

Select item 14659199777.

rs1465919977 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:43258218 (GRCh38)
19:43762370 (GRCh37)
Canonical SPDI:: NC_000019.10:43258217:C:G
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (GnomAD_exomes)
G=0.000019/5 (TOPMED)
G=0.00003/4 (GnomAD)
HGVS:: NC_000019.10:g.43258218C>G, NC_000019.9:g.43762370C>G, XM_005259075.5:c.948G>C, NM_002784.5:c.1227G>C, NM_002784.4:c.1227G>C, NM_002784.3:c.1227G>C, XM_017027007.3:c.1227G>C, XM_017027007.2:c.1227G>C, XM_017027007.1:c.1227G>C, NM_001301708.2:c.948G>C, NM_001301708.1:c.948G>C, NM_001301707.2:c.948G>C, NM_001301707.1:c.948G>C, NM_001301709.2:c.669G>C, NM_001301709.1:c.669G>C, NM_001411075.1:c.948G>C, XP_005259132.1:p.Met316Ile, NP_002775.3:p.Met409Ile, XP_016882496.1:p.Met409Ile, NP_001288637.1:p.Met316Ile, NP_001288636.1:p.Met316Ile, NP_001288638.1:p.Met223Ile

Select item 14644772588.

rs1464477258 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:43269402 (GRCh38)
19:43773554 (GRCh37)
Canonical SPDI:: NC_000019.10:43269401:T:A
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000019.10:g.43269402T>A, NC_000019.9:g.43773554T>A, XM_005259075.5:c.30A>T, NM_002784.5:c.30A>T, NM_002784.4:c.30A>T, NM_002784.3:c.30A>T, XM_017027007.3:c.30A>T, XM_017027007.2:c.30A>T, XM_017027007.1:c.30A>T, NM_001301708.2:c.30A>T, NM_001301708.1:c.30A>T, NM_001301707.2:c.30A>T, NM_001301707.1:c.30A>T, NM_001301709.2:c.30A>T, NM_001301709.1:c.30A>T, NM_001411075.1:c.30A>T

Select item 14619191619.

rs1461919161 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:43253641 (GRCh38)
19:43757793 (GRCh37)
Canonical SPDI:: NC_000019.10:43253640:A:G
Gene:: PSG9 (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000019.10:g.43253641A>G, NC_000019.9:g.43757793A>G, NM_002784.5:c.1249T>C, NM_002784.4:c.1249T>C, NM_002784.3:c.1249T>C, NM_001301708.2:c.970T>C, NM_001301708.1:c.970T>C, NM_001301707.2:c.970T>C, NM_001301707.1:c.970T>C, NM_001301709.2:c.691T>C, NM_001301709.1:c.691T>C, NP_002775.3:p.Cys417Arg, NP_001288637.1:p.Cys324Arg, NP_001288636.1:p.Cys324Arg, NP_001288638.1:p.Cys231Arg

Select item 145332354510.

rs1453323545 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:43267949 (GRCh38)
19:43772101 (GRCh37)
Canonical SPDI:: NC_000019.10:43267948:T:C
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.43267949T>C, NC_000019.9:g.43772101T>C, XM_005259075.5:c.265A>G, NM_002784.5:c.265A>G, NM_002784.4:c.265A>G, NM_002784.3:c.265A>G, XM_017027007.3:c.265A>G, XM_017027007.2:c.265A>G, XM_017027007.1:c.265A>G, NM_001301708.2:c.265A>G, NM_001301708.1:c.265A>G, NM_001301707.2:c.265A>G, NM_001301707.1:c.265A>G, NM_001301709.2:c.265A>G, NM_001301709.1:c.265A>G, NM_001411075.1:c.265A>G, XP_005259132.1:p.Ile89Val, NP_002775.3:p.Ile89Val, XP_016882496.1:p.Ile89Val, NP_001288637.1:p.Ile89Val, NP_001288636.1:p.Ile89Val, NP_001288638.1:p.Ile89Val

Select item 145286711511.

rs1452867115 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:43258455 (GRCh38)
19:43762607 (GRCh37)
Canonical SPDI:: NC_000019.10:43258454:A:G
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.43258455A>G, NC_000019.9:g.43762607A>G, XM_005259075.5:c.711T>C, NM_002784.5:c.990T>C, NM_002784.4:c.990T>C, NM_002784.3:c.990T>C, XM_017027007.3:c.990T>C, XM_017027007.2:c.990T>C, XM_017027007.1:c.990T>C, NM_001301708.2:c.711T>C, NM_001301708.1:c.711T>C, NM_001301707.2:c.711T>C, NM_001301707.1:c.711T>C, NM_001301709.2:c.432T>C, NM_001301709.1:c.432T>C, NM_001411075.1:c.711T>C

Select item 145278473712.

rs1452784737 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 19:43258243 (GRCh38)
19:43762396 (GRCh37)
Canonical SPDI:: NC_000019.10:43258243:T:TT
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.43258244dup, NC_000019.9:g.43762396dup, XM_005259075.5:c.922dup, NM_002784.5:c.1201dup, NM_002784.4:c.1201dup, NM_002784.3:c.1201dup, XM_017027007.3:c.1201dup, XM_017027007.2:c.1201dup, XM_017027007.1:c.1201dup, NM_001301708.2:c.922dup, NM_001301708.1:c.922dup, NM_001301707.2:c.922dup, NM_001301707.1:c.922dup, NM_001301709.2:c.643dup, NM_001301709.1:c.643dup, NM_001411075.1:c.922dup, XP_005259132.1:p.Thr308fs, NP_002775.3:p.Thr401fs, XP_016882496.1:p.Thr401fs, NP_001288637.1:p.Thr308fs, NP_001288636.1:p.Thr308fs, NP_001288638.1:p.Thr215fs

Select item 144732866313.

rs1447328663 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:43258380 (GRCh38)
19:43762532 (GRCh37)
Canonical SPDI:: NC_000019.10:43258379:G:A
Gene:: PSG9 (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_000019.10:g.43258380G>A, NC_000019.9:g.43762532G>A, XM_005259075.5:c.786C>T, NM_002784.5:c.1065C>T, NM_002784.4:c.1065C>T, NM_002784.3:c.1065C>T, XM_017027007.3:c.1065C>T, XM_017027007.2:c.1065C>T, XM_017027007.1:c.1065C>T, NM_001301708.2:c.786C>T, NM_001301708.1:c.786C>T, NM_001301707.2:c.786C>T, NM_001301707.1:c.786C>T, NM_001301709.2:c.507C>T, NM_001301709.1:c.507C>T, NM_001411075.1:c.786C>T

Select item 144480491614.

rs1444804916 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:43268034 (GRCh38)
19:43772186 (GRCh37)
Canonical SPDI:: NC_000019.10:43268033:C:G
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.43268034C>G, NC_000019.9:g.43772186C>G, XM_005259075.5:c.180G>C, NM_002784.5:c.180G>C, NM_002784.4:c.180G>C, NM_002784.3:c.180G>C, XM_017027007.3:c.180G>C, XM_017027007.2:c.180G>C, XM_017027007.1:c.180G>C, NM_001301708.2:c.180G>C, NM_001301708.1:c.180G>C, NM_001301707.2:c.180G>C, NM_001301707.1:c.180G>C, NM_001301709.2:c.180G>C, NM_001301709.1:c.180G>C, NM_001411075.1:c.180G>C, XP_005259132.1:p.Gln60His, NP_002775.3:p.Gln60His, XP_016882496.1:p.Gln60His, NP_001288637.1:p.Gln60His, NP_001288636.1:p.Gln60His, NP_001288638.1:p.Gln60His

Select item 143955127215.

rs1439551272 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:43268007 (GRCh38)
19:43772159 (GRCh37)
Canonical SPDI:: NC_000019.10:43268006:T:C
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.43268007T>C, NC_000019.9:g.43772159T>C, XM_005259075.5:c.207A>G, NM_002784.5:c.207A>G, NM_002784.4:c.207A>G, NM_002784.3:c.207A>G, XM_017027007.3:c.207A>G, XM_017027007.2:c.207A>G, XM_017027007.1:c.207A>G, NM_001301708.2:c.207A>G, NM_001301708.1:c.207A>G, NM_001301707.2:c.207A>G, NM_001301707.1:c.207A>G, NM_001301709.2:c.207A>G, NM_001301709.1:c.207A>G, NM_001411075.1:c.207A>G

Select item 143849122416.

rs1438491224 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:43269370 (GRCh38)
19:43773522 (GRCh37)
Canonical SPDI:: NC_000019.10:43269369:G:C
Gene:: PSG9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.43269370G>C, NC_000019.9:g.43773522G>C, XM_005259075.5:c.62C>G, NM_002784.5:c.62C>G, NM_002784.4:c.62C>G, NM_002784.3:c.62C>G, XM_017027007.3:c.62C>G, XM_017027007.2:c.62C>G, XM_017027007.1:c.62C>G, NM_001301708.2:c.62C>G, NM_001301708.1:c.62C>G, NM_001301707.2:c.62C>G, NM_001301707.1:c.62C>G, NM_001301709.2:c.62C>G, NM_001301709.1:c.62C>G, NM_001411075.1:c.62C>G, XP_005259132.1:p.Thr21Arg, NP_002775.3:p.Thr21Arg, XP_016882496.1:p.Thr21Arg, NP_001288637.1:p.Thr21Arg, NP_001288636.1:p.Thr21Arg, NP_001288638.1:p.Thr21Arg

Select item 143799814917.

rs1437998149 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:43267944 (GRCh38)
19:43772096 (GRCh37)
Canonical SPDI:: NC_000019.10:43267943:T:C
Gene:: PSG9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.43267944T>C, NC_000019.9:g.43772096T>C, XM_005259075.5:c.270A>G, NM_002784.5:c.270A>G, NM_002784.4:c.270A>G, NM_002784.3:c.270A>G, XM_017027007.3:c.270A>G, XM_017027007.2:c.270A>G, XM_017027007.1:c.270A>G, NM_001301708.2:c.270A>G, NM_001301708.1:c.270A>G, NM_001301707.2:c.270A>G, NM_001301707.1:c.270A>G, NM_001301709.2:c.270A>G, NM_001301709.1:c.270A>G, NM_001411075.1:c.270A>G, XP_005259132.1:p.Ile90Met, NP_002775.3:p.Ile90Met, XP_016882496.1:p.Ile90Met, NP_001288637.1:p.Ile90Met, NP_001288636.1:p.Ile90Met, NP_001288638.1:p.Ile90Met

Select item 143178065718.

rs1431780657 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:43267992 (GRCh38)
19:43772144 (GRCh37)
Canonical SPDI:: NC_000019.10:43267991:G:T
Gene:: PSG9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.43267992G>T, NC_000019.9:g.43772144G>T, XM_005259075.5:c.222C>A, NM_002784.5:c.222C>A, NM_002784.4:c.222C>A, NM_002784.3:c.222C>A, XM_017027007.3:c.222C>A, XM_017027007.2:c.222C>A, XM_017027007.1:c.222C>A, NM_001301708.2:c.222C>A, NM_001301708.1:c.222C>A, NM_001301707.2:c.222C>A, NM_001301707.1:c.222C>A, NM_001301709.2:c.222C>A, NM_001301709.1:c.222C>A, NM_001411075.1:c.222C>A, XP_005259132.1:p.Asp74Glu, NP_002775.3:p.Asp74Glu, XP_016882496.1:p.Asp74Glu, NP_001288637.1:p.Asp74Glu, NP_001288636.1:p.Asp74Glu, NP_001288638.1:p.Asp74Glu

Select item 143134567619.

rs1431345676 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:43267830 (GRCh38)
19:43771982 (GRCh37)
Canonical SPDI:: NC_000019.10:43267829:A:G
Gene:: PSG9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.43267830A>G, NC_000019.9:g.43771982A>G, XM_005259075.5:c.384T>C, NM_002784.5:c.384T>C, NM_002784.4:c.384T>C, NM_002784.3:c.384T>C, XM_017027007.3:c.384T>C, XM_017027007.2:c.384T>C, XM_017027007.1:c.384T>C, NM_001301708.2:c.384T>C, NM_001301708.1:c.384T>C, NM_001301707.2:c.384T>C, NM_001301707.1:c.384T>C, NM_001301709.2:c.384T>C, NM_001301709.1:c.384T>C, NM_001411075.1:c.384T>C

Select item 143118191520.

rs1431181915 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:43258365 (GRCh38)
19:43762517 (GRCh37)
Canonical SPDI:: NC_000019.10:43258364:T:C
Gene:: PSG9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.43258365T>C, NC_000019.9:g.43762517T>C, XM_005259075.5:c.801A>G, NM_002784.5:c.1080A>G, NM_002784.4:c.1080A>G, NM_002784.3:c.1080A>G, XM_017027007.3:c.1080A>G, XM_017027007.2:c.1080A>G, XM_017027007.1:c.1080A>G, NM_001301708.2:c.801A>G, NM_001301708.1:c.801A>G, NM_001301707.2:c.801A>G, NM_001301707.1:c.801A>G, NM_001301709.2:c.522A>G, NM_001301709.1:c.522A>G, NM_001411075.1:c.801A>G

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