SNP Links for Protein (Select 410442518) - SNP

Links from Protein

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Select item 14903516881.

rs1490351688 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55096105 (GRCh38)
19:55607473 (GRCh37)
Canonical SPDI:: NC_000019.10:55096104:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.55096105C>T, NC_000019.9:g.55607473C>T, XM_005259013.5:c.1099G>A, XM_005259013.4:c.1099G>A, XM_005259013.3:c.1099G>A, XM_005259013.2:c.1099G>A, XM_005259013.1:c.1099G>A, NM_017607.4:c.1099G>A, NM_017607.3:c.1099G>A, XM_011527045.3:c.1099G>A, XM_011527045.2:c.1099G>A, XM_011527045.1:c.1099G>A, NM_001271618.2:c.1099G>A, NM_001271618.1:c.1099G>A, XR_007066879.1:n.1193G>A, XP_005259070.1:p.Gly367Arg, NP_060077.1:p.Gly367Arg, XP_011525347.1:p.Gly367Arg, NP_001258547.1:p.Gly367Arg

Select item 14899357632.

rs1489935763 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55098808 (GRCh38)
19:55610176 (GRCh37)
Canonical SPDI:: NC_000019.10:55098807:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000085/3 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.55098808C>T, NC_000019.9:g.55610176C>T, XM_005259013.5:c.927G>A, XM_005259013.4:c.927G>A, XM_005259013.3:c.927G>A, XM_005259013.2:c.927G>A, XM_005259013.1:c.927G>A, NM_017607.4:c.927G>A, NM_017607.3:c.927G>A, XM_011527045.3:c.927G>A, XM_011527045.2:c.927G>A, XM_011527045.1:c.927G>A, NM_001271618.2:c.927G>A, NM_001271618.1:c.927G>A, XR_007066879.1:n.1021G>A

Select item 14890510983.

rs1489051098 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:55112688 (GRCh38)
19:55624056 (GRCh37)
Canonical SPDI:: NC_000019.10:55112687:G:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.55112688G>T, NC_000019.9:g.55624056G>T, XM_005259013.5:c.429C>A, XM_005259013.4:c.429C>A, XM_005259013.3:c.429C>A, XM_005259013.2:c.429C>A, XM_005259013.1:c.429C>A, NM_017607.4:c.429C>A, NM_017607.3:c.429C>A, XM_011527045.3:c.429C>A, XM_011527045.2:c.429C>A, XM_011527045.1:c.429C>A, NM_001271618.2:c.429C>A, NM_001271618.1:c.429C>A, XR_007066879.1:n.523C>A

Select item 14878311184.

rs1487831118 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:55117333 (GRCh38)
19:55628701 (GRCh37)
Canonical SPDI:: NC_000019.10:55117332:G:A
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.55117333G>A, NC_000019.9:g.55628701G>A, XM_005259013.5:c.211C>T, XM_005259013.4:c.211C>T, XM_005259013.3:c.211C>T, XM_005259013.2:c.211C>T, XM_005259013.1:c.211C>T, NM_017607.4:c.211C>T, NM_017607.3:c.211C>T, XM_011527045.3:c.211C>T, XM_011527045.2:c.211C>T, XM_011527045.1:c.211C>T, NM_001271618.2:c.211C>T, NM_001271618.1:c.211C>T, XR_007066879.1:n.305C>T

Select item 14875519175.

rs1487551917 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:55094668 (GRCh38)
19:55606036 (GRCh37)
Canonical SPDI:: NC_000019.10:55094667:G:C
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.55094668G>C, NC_000019.9:g.55606036G>C, XM_005259013.5:c.1585C>G, XM_005259013.4:c.1585C>G, XM_005259013.3:c.1585C>G, XM_005259013.2:c.1585C>G, XM_005259013.1:c.1585C>G, NM_017607.4:c.1585C>G, NM_017607.3:c.1585C>G, XM_011527045.3:c.1582C>G, XM_011527045.2:c.1582C>G, XM_011527045.1:c.1582C>G, NM_001271618.2:c.1582C>G, NM_001271618.1:c.1582C>G, XR_007066879.1:n.1679C>G, XP_005259070.1:p.Arg529Gly, NP_060077.1:p.Arg529Gly, XP_011525347.1:p.Arg528Gly, NP_001258547.1:p.Arg528Gly

Select item 14858972256.

rs1485897225 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:55092263 (GRCh38)
19:55603631 (GRCh37)
Canonical SPDI:: NC_000019.10:55092262:G:A
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.55092263G>A, NC_000019.9:g.55603631G>A, XM_005259013.5:c.2116C>T, XM_005259013.4:c.2116C>T, XM_005259013.3:c.2116C>T, XM_005259013.2:c.2116C>T, XM_005259013.1:c.2116C>T, NM_017607.4:c.2119C>T, NM_017607.3:c.2119C>T, XM_011527045.3:c.2116C>T, XM_011527045.2:c.2116C>T, XM_011527045.1:c.2116C>T, NM_001271618.2:c.2113C>T, NM_001271618.1:c.2113C>T, XR_007066879.1:n.2110C>T, XP_005259070.1:p.Arg706Trp, NP_060077.1:p.Arg707Trp, XP_011525347.1:p.Arg706Trp, NP_001258547.1:p.Arg705Trp

Select item 14857181587.

rs1485718158 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55117236 (GRCh38)
19:55628604 (GRCh37)
Canonical SPDI:: NC_000019.10:55117235:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.55117236C>T, NC_000019.9:g.55628604C>T, XM_005259013.5:c.308G>A, XM_005259013.4:c.308G>A, XM_005259013.3:c.308G>A, XM_005259013.2:c.308G>A, XM_005259013.1:c.308G>A, NM_017607.4:c.308G>A, NM_017607.3:c.308G>A, XM_011527045.3:c.308G>A, XM_011527045.2:c.308G>A, XM_011527045.1:c.308G>A, NM_001271618.2:c.308G>A, NM_001271618.1:c.308G>A, XR_007066879.1:n.402G>A, XP_005259070.1:p.Ser103Asn, NP_060077.1:p.Ser103Asn, XP_011525347.1:p.Ser103Asn, NP_001258547.1:p.Ser103Asn

Select item 14855236518.

rs1485523651 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55117510 (GRCh38)
19:55628878 (GRCh37)
Canonical SPDI:: NC_000019.10:55117509:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.55117510C>T, NC_000019.9:g.55628878C>T, XM_005259013.5:c.34G>A, XM_005259013.4:c.34G>A, XM_005259013.3:c.34G>A, XM_005259013.2:c.34G>A, XM_005259013.1:c.34G>A, NM_017607.4:c.34G>A, NM_017607.3:c.34G>A, XM_011527045.3:c.34G>A, XM_011527045.2:c.34G>A, XM_011527045.1:c.34G>A, NM_001271618.2:c.34G>A, NM_001271618.1:c.34G>A, XR_007066879.1:n.128G>A, XP_005259070.1:p.Gly12Arg, NP_060077.1:p.Gly12Arg, XP_011525347.1:p.Gly12Arg, NP_001258547.1:p.Gly12Arg

Select item 14842957739.

rs1484295773 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55103534 (GRCh38)
19:55614902 (GRCh37)
Canonical SPDI:: NC_000019.10:55103533:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.55103534C>T, NC_000019.9:g.55614902C>T, XM_005259013.5:c.606G>A, XM_005259013.4:c.606G>A, XM_005259013.3:c.606G>A, XM_005259013.2:c.606G>A, XM_005259013.1:c.606G>A, NM_017607.4:c.606G>A, NM_017607.3:c.606G>A, XM_011527045.3:c.606G>A, XM_011527045.2:c.606G>A, XM_011527045.1:c.606G>A, NM_001271618.2:c.606G>A, NM_001271618.1:c.606G>A, XR_007066879.1:n.700G>A

Select item 148400517310.

rs1484005173 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55094415 (GRCh38)
19:55605783 (GRCh37)
Canonical SPDI:: NC_000019.10:55094414:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000019.10:g.55094415C>T, NC_000019.9:g.55605783C>T, XM_005259013.5:c.1613G>A, XM_005259013.4:c.1613G>A, XM_005259013.3:c.1613G>A, XM_005259013.2:c.1613G>A, XM_005259013.1:c.1613G>A, NM_017607.4:c.1613G>A, NM_017607.3:c.1613G>A, XM_011527045.3:c.1610G>A, XM_011527045.2:c.1610G>A, XM_011527045.1:c.1610G>A, NM_001271618.2:c.1610G>A, NM_001271618.1:c.1610G>A, XR_007066879.1:n.1707G>A, XP_005259070.1:p.Arg538Gln, NP_060077.1:p.Arg538Gln, XP_011525347.1:p.Arg537Gln, NP_001258547.1:p.Arg537Gln

Select item 148375662611.

rs1483756626 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55094357 (GRCh38)
19:55605725 (GRCh37)
Canonical SPDI:: NC_000019.10:55094356:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000019.10:g.55094357C>T, NC_000019.9:g.55605725C>T, XM_005259013.5:c.1671G>A, XM_005259013.4:c.1671G>A, XM_005259013.3:c.1671G>A, XM_005259013.2:c.1671G>A, XM_005259013.1:c.1671G>A, NM_017607.4:c.1671G>A, NM_017607.3:c.1671G>A, XM_011527045.3:c.1668G>A, XM_011527045.2:c.1668G>A, XM_011527045.1:c.1668G>A, NM_001271618.2:c.1668G>A, NM_001271618.1:c.1668G>A, XR_007066879.1:n.1765G>A

Select item 148285086012.

rs1482850860 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55117522 (GRCh38)
19:55628890 (GRCh37)
Canonical SPDI:: NC_000019.10:55117521:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_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_000019.10:g.55117522C>T, NC_000019.9:g.55628890C>T, XM_005259013.5:c.22G>A, XM_005259013.4:c.22G>A, XM_005259013.3:c.22G>A, XM_005259013.2:c.22G>A, XM_005259013.1:c.22G>A, NM_017607.4:c.22G>A, NM_017607.3:c.22G>A, XM_011527045.3:c.22G>A, XM_011527045.2:c.22G>A, XM_011527045.1:c.22G>A, NM_001271618.2:c.22G>A, NM_001271618.1:c.22G>A, XR_007066879.1:n.116G>A, XP_005259070.1:p.Ala8Thr, NP_060077.1:p.Ala8Thr, XP_011525347.1:p.Ala8Thr, NP_001258547.1:p.Ala8Thr

Select item 148178556513.

rs1481785565 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:55098822 (GRCh38)
19:55610190 (GRCh37)
Canonical SPDI:: NC_000019.10:55098821:G:A
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000014/2 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000019.10:g.55098822G>A, NC_000019.9:g.55610190G>A, XM_005259013.5:c.913C>T, XM_005259013.4:c.913C>T, XM_005259013.3:c.913C>T, XM_005259013.2:c.913C>T, XM_005259013.1:c.913C>T, NM_017607.4:c.913C>T, NM_017607.3:c.913C>T, XM_011527045.3:c.913C>T, XM_011527045.2:c.913C>T, XM_011527045.1:c.913C>T, NM_001271618.2:c.913C>T, NM_001271618.1:c.913C>T, XR_007066879.1:n.1007C>T

Select item 148058732514.

rs1480587325 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:55096059 (GRCh38)
19:55607427 (GRCh37)
Canonical SPDI:: NC_000019.10:55096058:C:G
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.55096059C>G, NC_000019.9:g.55607427C>G, XM_005259013.5:c.1145G>C, XM_005259013.4:c.1145G>C, XM_005259013.3:c.1145G>C, XM_005259013.2:c.1145G>C, XM_005259013.1:c.1145G>C, NM_017607.4:c.1145G>C, NM_017607.3:c.1145G>C, XM_011527045.3:c.1145G>C, XM_011527045.2:c.1145G>C, XM_011527045.1:c.1145G>C, NM_001271618.2:c.1145G>C, NM_001271618.1:c.1145G>C, XR_007066879.1:n.1239G>C, XP_005259070.1:p.Gly382Ala, NP_060077.1:p.Gly382Ala, XP_011525347.1:p.Gly382Ala, NP_001258547.1:p.Gly382Ala

Select item 148010732515.

rs1480107325 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:55117495 (GRCh38)
19:55628863 (GRCh37)
Canonical SPDI:: NC_000019.10:55117494:C:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.0001/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.55117495C>T, NC_000019.9:g.55628863C>T, XM_005259013.5:c.49G>A, XM_005259013.4:c.49G>A, XM_005259013.3:c.49G>A, XM_005259013.2:c.49G>A, XM_005259013.1:c.49G>A, NM_017607.4:c.49G>A, NM_017607.3:c.49G>A, XM_011527045.3:c.49G>A, XM_011527045.2:c.49G>A, XM_011527045.1:c.49G>A, NM_001271618.2:c.49G>A, NM_001271618.1:c.49G>A, XR_007066879.1:n.143G>A, XP_005259070.1:p.Ala17Thr, NP_060077.1:p.Ala17Thr, XP_011525347.1:p.Ala17Thr, NP_001258547.1:p.Ala17Thr

Select item 147993657316.

rs1479936573 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:55095347 (GRCh38)
19:55606715 (GRCh37)
Canonical SPDI:: NC_000019.10:55095346:G:A
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.55095347G>A, NC_000019.9:g.55606715G>A, XM_005259013.5:c.1398C>T, XM_005259013.4:c.1398C>T, XM_005259013.3:c.1398C>T, XM_005259013.2:c.1398C>T, XM_005259013.1:c.1398C>T, NM_017607.4:c.1398C>T, NM_017607.3:c.1398C>T, XM_011527045.3:c.1395C>T, XM_011527045.2:c.1395C>T, XM_011527045.1:c.1395C>T, NM_001271618.2:c.1395C>T, NM_001271618.1:c.1395C>T, XR_007066879.1:n.1492C>T

Select item 147974130117.

rs1479741301 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:55096126 (GRCh38)
19:55607494 (GRCh37)
Canonical SPDI:: NC_000019.10:55096125:A:G
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.55096126A>G, NC_000019.9:g.55607494A>G, XM_005259013.5:c.1078T>C, XM_005259013.4:c.1078T>C, XM_005259013.3:c.1078T>C, XM_005259013.2:c.1078T>C, XM_005259013.1:c.1078T>C, NM_017607.4:c.1078T>C, NM_017607.3:c.1078T>C, XM_011527045.3:c.1078T>C, XM_011527045.2:c.1078T>C, XM_011527045.1:c.1078T>C, NM_001271618.2:c.1078T>C, NM_001271618.1:c.1078T>C, XR_007066879.1:n.1172T>C, XP_005259070.1:p.Ser360Pro, NP_060077.1:p.Ser360Pro, XP_011525347.1:p.Ser360Pro, NP_001258547.1:p.Ser360Pro

Select item 147873707418.

rs1478737074 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:55092253 (GRCh38)
19:55603621 (GRCh37)
Canonical SPDI:: NC_000019.10:55092252:T:G
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_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.55092253T>G, NC_000019.9:g.55603621T>G, XM_005259013.5:c.2126A>C, XM_005259013.4:c.2126A>C, XM_005259013.3:c.2126A>C, XM_005259013.2:c.2126A>C, XM_005259013.1:c.2126A>C, NM_017607.4:c.2129A>C, NM_017607.3:c.2129A>C, XM_011527045.3:c.2126A>C, XM_011527045.2:c.2126A>C, XM_011527045.1:c.2126A>C, NM_001271618.2:c.2123A>C, NM_001271618.1:c.2123A>C, XR_007066879.1:n.2120A>C, XP_005259070.1:p.Gln709Pro, NP_060077.1:p.Gln710Pro, XP_011525347.1:p.Gln709Pro, NP_001258547.1:p.Gln708Pro

Select item 147818833519.

rs1478188335 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:55117278 (GRCh38)
19:55628646 (GRCh37)
Canonical SPDI:: NC_000019.10:55117277:G:C
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.55117278G>C, NC_000019.9:g.55628646G>C, XM_005259013.5:c.266C>G, XM_005259013.4:c.266C>G, XM_005259013.3:c.266C>G, XM_005259013.2:c.266C>G, XM_005259013.1:c.266C>G, NM_017607.4:c.266C>G, NM_017607.3:c.266C>G, XM_011527045.3:c.266C>G, XM_011527045.2:c.266C>G, XM_011527045.1:c.266C>G, NM_001271618.2:c.266C>G, NM_001271618.1:c.266C>G, XR_007066879.1:n.360C>G, XP_005259070.1:p.Pro89Arg, NP_060077.1:p.Pro89Arg, XP_011525347.1:p.Pro89Arg, NP_001258547.1:p.Pro89Arg

Select item 147769461520.

rs1477694615 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:55099062 (GRCh38)
19:55610430 (GRCh37)
Canonical SPDI:: NC_000019.10:55099061:G:T
Gene:: PPP1R12C (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.55099062G>T, NC_000019.9:g.55610430G>T, XM_005259013.5:c.765C>A, XM_005259013.4:c.765C>A, XM_005259013.3:c.765C>A, XM_005259013.2:c.765C>A, XM_005259013.1:c.765C>A, NM_017607.4:c.765C>A, NM_017607.3:c.765C>A, XM_011527045.3:c.765C>A, XM_011527045.2:c.765C>A, XM_011527045.1:c.765C>A, NM_001271618.2:c.765C>A, NM_001271618.1:c.765C>A, XR_007066879.1:n.859C>A

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