SNP Links for Protein (Select 211971058) - SNP - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Protein

Items: 1 to 20 of 489

<< First< Prev

Page of 25

Select item 14900161501.

rs1490016150 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:130127509 (GRCh38)
9:132889788 (GRCh37)
Canonical SPDI:: NC_000009.12:130127508:G:T
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.130127509G>T, NC_000009.11:g.132889788G>T, NM_020960.5:c.1383G>T, NM_020960.4:c.1383G>T, XM_017014953.3:c.1383G>T, XM_017014953.2:c.1383G>T, XM_017014953.1:c.1383G>T, NM_001136557.2:c.1527G>T, NM_001136557.1:c.1527G>T, NM_001136558.2:c.1440G>T, NM_001136558.1:c.1440G>T, NM_001287346.2:c.816G>T, NM_001287346.1:c.816G>T, XR_007061336.1:n.1467G>T, NP_066011.2:p.Arg461Ser, XP_016870442.1:p.Arg461Ser, NP_001130029.1:p.Arg509Ser, NP_001130030.1:p.Arg480Ser, NP_001274275.1:p.Arg272Ser

Select item 14889465062.

rs1488946506 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:130053947 (GRCh38)
9:132816226 (GRCh37)
Canonical SPDI:: NC_000009.12:130053946:G:C
Gene:: FNBP1 (Varview), GPR107 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant,upstream_transcript_variant,coding_sequence_variant,synonymous_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.130053947G>C, NC_000009.11:g.132816226G>C, NM_020960.5:c.15G>C, NM_020960.4:c.15G>C, XM_017014953.3:c.15G>C, XM_017014953.2:c.15G>C, XM_017014953.1:c.15G>C, NM_001136557.2:c.15G>C, NM_001136557.1:c.15G>C, NM_001136558.2:c.15G>C, NM_001136558.1:c.15G>C, NM_001287346.2:c.-549G>C, NM_001287346.1:c.-549G>C, XR_007061336.1:n.42G>C

Select item 14865953123.

rs1486595312 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:130099505 (GRCh38)
9:132861784 (GRCh37)
Canonical SPDI:: NC_000009.12:130099504:C:T
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.130099505C>T, NC_000009.11:g.132861784C>T, NM_020960.5:c.912C>T, NM_020960.4:c.912C>T, XM_017014953.3:c.912C>T, XM_017014953.2:c.912C>T, XM_017014953.1:c.912C>T, NM_001136557.2:c.912C>T, NM_001136557.1:c.912C>T, NM_001136558.2:c.912C>T, NM_001136558.1:c.912C>T, NM_001287346.2:c.345C>T, NM_001287346.1:c.345C>T, XR_007061336.1:n.939C>T

Select item 14835322054.

rs1483532205 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:130128744 (GRCh38)
9:132891023 (GRCh37)
Canonical SPDI:: NC_000009.12:130128743:C:A
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.130128744C>A, NC_000009.11:g.132891023C>A, NM_020960.5:c.1545C>A, NM_020960.4:c.1545C>A, XM_017014953.3:c.1545C>A, XM_017014953.2:c.1545C>A, XM_017014953.1:c.1545C>A, NM_001136557.2:c.1689C>A, NM_001136557.1:c.1689C>A, NM_001136558.2:c.1602C>A, NM_001136558.1:c.1602C>A, NM_001287346.2:c.978C>A, NM_001287346.1:c.978C>A, XR_007061336.1:n.1629C>A, NP_066011.2:p.Asp515Glu, XP_016870442.1:p.Asp515Glu, NP_001130029.1:p.Asp563Glu, NP_001130030.1:p.Asp534Glu, NP_001274275.1:p.Asp326Glu

Select item 14831065665.

rs1483106566 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:130124961 (GRCh38)
9:132887240 (GRCh37)
Canonical SPDI:: NC_000009.12:130124960:C:G
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
HGVS:: NC_000009.12:g.130124961C>G, NC_000009.11:g.132887240C>G, NM_020960.5:c.1353C>G, NM_020960.4:c.1353C>G, XM_017014953.3:c.1353C>G, XM_017014953.2:c.1353C>G, XM_017014953.1:c.1353C>G, NM_001136557.2:c.1497C>G, NM_001136557.1:c.1497C>G, NM_001136558.2:c.1410C>G, NM_001136558.1:c.1410C>G, NM_001287346.2:c.786C>G, NM_001287346.1:c.786C>G, XR_007061336.1:n.1437C>G

Select item 14824113766.

rs1482411376 [Homo sapiens]

Variant type:: DELINS
Alleles:: GCCT>- [Show Flanks]
Chromosome:: 9:130114633 (GRCh38)
9:132876912 (GRCh37)
Canonical SPDI:: NC_000009.12:130114629:CCTGCCT:CCT
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: CCT=0./0 (ALFA)
HGVS:: NC_000009.12:g.130114633_130114636del, NC_000009.11:g.132876912_132876915del, NM_001136557.2:c.1420_1423del, NM_001136557.1:c.1420_1423del, NP_001130029.1:p.Ala474fs

Select item 14818073407.

rs1481807340 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:130092328 (GRCh38)
9:132854607 (GRCh37)
Canonical SPDI:: NC_000009.12:130092327:C:T
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.130092328C>T, NC_000009.11:g.132854607C>T, NM_020960.5:c.810C>T, NM_020960.4:c.810C>T, XM_017014953.3:c.810C>T, XM_017014953.2:c.810C>T, XM_017014953.1:c.810C>T, NM_001136557.2:c.810C>T, NM_001136557.1:c.810C>T, NM_001136558.2:c.810C>T, NM_001136558.1:c.810C>T, NM_001287346.2:c.243C>T, NM_001287346.1:c.243C>T, XR_007061336.1:n.837C>T

Select item 14817819818.

rs1481781981 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:130083601 (GRCh38)
9:132845880 (GRCh37)
Canonical SPDI:: NC_000009.12:130083600:A:C
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.130083601A>C, NC_000009.11:g.132845880A>C, NM_020960.5:c.563A>C, NM_020960.4:c.563A>C, XM_017014953.3:c.563A>C, XM_017014953.2:c.563A>C, XM_017014953.1:c.563A>C, NM_001136557.2:c.563A>C, NM_001136557.1:c.563A>C, NM_001136558.2:c.563A>C, NM_001136558.1:c.563A>C, NM_001287346.2:c.-5A>C, NM_001287346.1:c.-5A>C, XR_007061336.1:n.590A>C, NP_066011.2:p.Lys188Thr, XP_016870442.1:p.Lys188Thr, NP_001130029.1:p.Lys188Thr, NP_001130030.1:p.Lys188Thr

Select item 14816029439.

rs1481602943 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:130128677 (GRCh38)
9:132890956 (GRCh37)
Canonical SPDI:: NC_000009.12:130128676:T:C
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.130128677T>C, NC_000009.11:g.132890956T>C, NM_020960.5:c.1478T>C, NM_020960.4:c.1478T>C, XM_017014953.3:c.1478T>C, XM_017014953.2:c.1478T>C, XM_017014953.1:c.1478T>C, NM_001136557.2:c.1622T>C, NM_001136557.1:c.1622T>C, NM_001136558.2:c.1535T>C, NM_001136558.1:c.1535T>C, NM_001287346.2:c.911T>C, NM_001287346.1:c.911T>C, XR_007061336.1:n.1562T>C, NP_066011.2:p.Leu493Pro, XP_016870442.1:p.Leu493Pro, NP_001130029.1:p.Leu541Pro, NP_001130030.1:p.Leu512Pro, NP_001274275.1:p.Leu304Pro

Select item 147832297510.

rs1478322975 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:130114601 (GRCh38)
9:132876880 (GRCh37)
Canonical SPDI:: NC_000009.12:130114600:A:G
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000084/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.130114601A>G, NC_000009.11:g.132876880A>G, NM_001136557.2:c.1388A>G, NM_001136557.1:c.1388A>G, NP_001130029.1:p.Asp463Gly

Select item 147725980811.

rs1477259808 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:130092333 (GRCh38)
9:132854612 (GRCh37)
Canonical SPDI:: NC_000009.12:130092332:T:C
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.130092333T>C, NC_000009.11:g.132854612T>C, NM_020960.5:c.815T>C, NM_020960.4:c.815T>C, XM_017014953.3:c.815T>C, XM_017014953.2:c.815T>C, XM_017014953.1:c.815T>C, NM_001136557.2:c.815T>C, NM_001136557.1:c.815T>C, NM_001136558.2:c.815T>C, NM_001136558.1:c.815T>C, NM_001287346.2:c.248T>C, NM_001287346.1:c.248T>C, XR_007061336.1:n.842T>C, NP_066011.2:p.Phe272Ser, XP_016870442.1:p.Phe272Ser, NP_001130029.1:p.Phe272Ser, NP_001130030.1:p.Phe272Ser, NP_001274275.1:p.Phe83Ser

Select item 147539242012.

rs1475392420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:130099516 (GRCh38)
9:132861795 (GRCh37)
Canonical SPDI:: NC_000009.12:130099515:C:A
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.0001/1 (ALFA)
HGVS:: NC_000009.12:g.130099516C>A, NC_000009.11:g.132861795C>A, NM_020960.5:c.923C>A, NM_020960.4:c.923C>A, XM_017014953.3:c.923C>A, XM_017014953.2:c.923C>A, XM_017014953.1:c.923C>A, NM_001136557.2:c.923C>A, NM_001136557.1:c.923C>A, NM_001136558.2:c.923C>A, NM_001136558.1:c.923C>A, NM_001287346.2:c.356C>A, NM_001287346.1:c.356C>A, XR_007061336.1:n.950C>A, NP_066011.2:p.Ser308Tyr, XP_016870442.1:p.Ser308Tyr, NP_001130029.1:p.Ser308Tyr, NP_001130030.1:p.Ser308Tyr, NP_001274275.1:p.Ser119Tyr

Select item 147245024213.

rs1472450242 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:130092317 (GRCh38)
9:132854596 (GRCh37)
Canonical SPDI:: NC_000009.12:130092316:A:C
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.130092317A>C, NC_000009.11:g.132854596A>C, NM_020960.5:c.799A>C, NM_020960.4:c.799A>C, XM_017014953.3:c.799A>C, XM_017014953.2:c.799A>C, XM_017014953.1:c.799A>C, NM_001136557.2:c.799A>C, NM_001136557.1:c.799A>C, NM_001136558.2:c.799A>C, NM_001136558.1:c.799A>C, NM_001287346.2:c.232A>C, NM_001287346.1:c.232A>C, XR_007061336.1:n.826A>C, NP_066011.2:p.Ile267Leu, XP_016870442.1:p.Ile267Leu, NP_001130029.1:p.Ile267Leu, NP_001130030.1:p.Ile267Leu, NP_001274275.1:p.Ile78Leu

Select item 147212238214.

rs1472122382 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:130083578 (GRCh38)
9:132845857 (GRCh37)
Canonical SPDI:: NC_000009.12:130083577:T:C
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000031/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.130083578T>C, NC_000009.11:g.132845857T>C, NM_020960.5:c.540T>C, NM_020960.4:c.540T>C, XM_017014953.3:c.540T>C, XM_017014953.2:c.540T>C, XM_017014953.1:c.540T>C, NM_001136557.2:c.540T>C, NM_001136557.1:c.540T>C, NM_001136558.2:c.540T>C, NM_001136558.1:c.540T>C, NM_001287346.2:c.-28T>C, NM_001287346.1:c.-28T>C, XR_007061336.1:n.567T>C

Select item 147174276915.

rs1471742769 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTT>- [Show Flanks]
Chromosome:: 9:130076455 (GRCh38)
9:132838734 (GRCh37)
Canonical SPDI:: NC_000009.12:130076449:TTCTTCTT:TTCTT
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_deletion,5_prime_UTR_variant,non_coding_transcript_variant
HGVS:: NC_000009.12:g.130076452CTT[1], NC_000009.11:g.132838731CTT[1], NM_020960.5:c.296CTT[1], NM_020960.4:c.296CTT[1], XM_017014953.3:c.296CTT[1], XM_017014953.2:c.296CTT[1], XM_017014953.1:c.296CTT[1], NM_001136557.2:c.296CTT[1], NM_001136557.1:c.296CTT[1], NM_001136558.2:c.296CTT[1], NM_001136558.1:c.296CTT[1], NM_001287346.2:c.-268CTT[1], NM_001287346.1:c.-268CTT[1], XR_007061336.1:n.323CTT[1], NP_066011.2:p.Ser100del, XP_016870442.1:p.Ser100del, NP_001130029.1:p.Ser100del, NP_001130030.1:p.Ser100del

Select item 146971206116.

rs1469712061 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACTTA>- [Show Flanks]
Chromosome:: 9:130124924 (GRCh38)
9:132887203 (GRCh37)
Canonical SPDI:: NC_000009.12:130124920:TTAACTTA:TTA
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.130124924_130124928del, NC_000009.11:g.132887203_132887207del, NM_020960.5:c.1316_1320del, NM_020960.4:c.1316_1320del, XM_017014953.3:c.1316_1320del, XM_017014953.2:c.1316_1320del, XM_017014953.1:c.1316_1320del, NM_001136557.2:c.1460_1464del, NM_001136557.1:c.1460_1464del, NM_001136558.2:c.1373_1377del, NM_001136558.1:c.1373_1377del, NM_001287346.2:c.749_753del, NM_001287346.1:c.749_753del, XR_007061336.1:n.1400_1404del, NP_066011.2:p.Asn439fs, XP_016870442.1:p.Asn439fs, NP_001130029.1:p.Asn487fs, NP_001130030.1:p.Asn458fs, NP_001274275.1:p.Asn250fs

Select item 146760339117.

rs1467603391 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:130104530 (GRCh38)
9:132866809 (GRCh37)
Canonical SPDI:: NC_000009.12:130104529:C:T
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.130104530C>T, NC_000009.11:g.132866809C>T, NM_020960.5:c.1242C>T, NM_020960.4:c.1242C>T, XM_017014953.3:c.1242C>T, XM_017014953.2:c.1242C>T, XM_017014953.1:c.1242C>T, NM_001136557.2:c.1242C>T, NM_001136557.1:c.1242C>T, NM_001136558.2:c.1242C>T, NM_001136558.1:c.1242C>T, NM_001287346.2:c.675C>T, NM_001287346.1:c.675C>T, XR_007061336.1:n.1269C>T

Select item 146716171718.

rs1467161717 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:130110397 (GRCh38)
9:132872676 (GRCh37)
Canonical SPDI:: NC_000009.12:130110396:G:A
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,intron_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.130110397G>A, NC_000009.11:g.132872676G>A, NM_001136557.2:c.1334G>A, NM_001136557.1:c.1334G>A, NM_001136558.2:c.1334G>A, NM_001136558.1:c.1334G>A, XR_007061336.1:n.1361G>A, NP_001130029.1:p.Arg445Lys, NP_001130030.1:p.Arg445Lys

Select item 146650392019.

rs1466503920 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:130110423 (GRCh38)
9:132872702 (GRCh37)
Canonical SPDI:: NC_000009.12:130110422:A:G
Gene:: GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.130110423A>G, NC_000009.11:g.132872702A>G, NM_001136557.2:c.1360A>G, NM_001136557.1:c.1360A>G, NM_001136558.2:c.1360A>G, NM_001136558.1:c.1360A>G, XR_007061336.1:n.1387A>G, NP_001130029.1:p.Ile454Val, NP_001130030.1:p.Ile454Val

Select item 146471516220.

rs1464715162 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:130053980 (GRCh38)
9:132816259 (GRCh37)
Canonical SPDI:: NC_000009.12:130053979:G:A
Gene:: FNBP1 (Varview), GPR107 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant,5_prime_UTR_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000043/1 (ALFA)
A=0.000007/1 (GnomAD_exomes)
A=0.000021/3 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.130053980G>A, NC_000009.11:g.132816259G>A, NM_020960.5:c.48G>A, NM_020960.4:c.48G>A, XM_017014953.3:c.48G>A, XM_017014953.2:c.48G>A, XM_017014953.1:c.48G>A, NM_001136557.2:c.48G>A, NM_001136557.1:c.48G>A, NM_001136558.2:c.48G>A, NM_001136558.1:c.48G>A, NM_001287346.2:c.-516G>A, NM_001287346.1:c.-516G>A, XR_007061336.1:n.75G>A

<< First< Prev

Page of 25

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Protein (Select 211971058) (489)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...