SNP Links for Protein (Select 4508045) - SNP

Links from Protein

Items: 1 to 20 of 755

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Select item 14902299041.

rs1490229904 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:21199589 (GRCh38)
16:21210910 (GRCh37)
Canonical SPDI:: NC_000016.10:21199588:C:G,NC_000016.10:21199588:C:T
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.21199589C>G, NC_000016.10:g.21199589C>T, NC_000016.9:g.21210910C>G, NC_000016.9:g.21210910C>T, NW_017852933.1:g.23280C>G, NW_017852933.1:g.23280C>T, NM_003460.2:c.1908G>C, NM_003460.2:c.1908G>A, NM_003460.1:c.1908G>C, NM_003460.1:c.1908G>A, NM_001376232.1:c.1908G>C, NM_001376232.1:c.1908G>A, NM_001376231.1:c.1881G>C, NM_001376231.1:c.1881G>A, NM_001290104.1:c.1881G>C, NM_001290104.1:c.1881G>A, NM_001376233.1:c.1908G>C, NM_001376233.1:c.1908G>A

Select item 14888538582.

rs1488853858 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:21201744 (GRCh38)
16:21213065 (GRCh37)
Canonical SPDI:: NC_000016.10:21201743:T:C
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21201744T>C, NC_000016.9:g.21213065T>C, NW_017852933.1:g.25435T>C, NM_003460.2:c.1466A>G, NM_003460.1:c.1466A>G, NM_001376232.1:c.1466A>G, NM_001376231.1:c.1439A>G, NR_164788.1:n.1493A>G, NM_001290104.1:c.1439A>G, NM_001376233.1:c.1466A>G, NP_003451.1:p.Lys489Arg, NP_001363161.1:p.Lys489Arg, NP_001363160.1:p.Lys480Arg, NP_001363162.1:p.Lys489Arg

Select item 14872427343.

rs1487242734 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 16:21204143 (GRCh38)
16:21215464 (GRCh37)
Canonical SPDI:: NC_000016.10:21204140:CACA:CA
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACA=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21204141CA[1], NC_000016.9:g.21215462CA[1], NW_017852933.1:g.27832CA[1], NM_003460.2:c.860_861del, NM_003460.1:c.860_861del, NM_001376232.1:c.860_861del, NM_001290104.1:c.860_861del, NM_001376231.1:c.860_861del, NR_164788.1:n.885TG[1], NM_001376233.1:c.860_861del, NP_003451.1:p.Val287fs, NP_001363161.1:p.Val287fs, NP_001363160.1:p.Val287fs, NP_001363162.1:p.Val287fs

Select item 14866612534.

rs1486661253 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:21204396 (GRCh38)
16:21215717 (GRCh37)
Canonical SPDI:: NC_000016.10:21204395:G:A
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.21204396G>A, NC_000016.9:g.21215717G>A, NW_017852933.1:g.28087G>A, NM_003460.2:c.702C>T, NM_003460.1:c.702C>T, NM_001376232.1:c.702C>T, NM_001376231.1:c.702C>T, NR_164788.1:n.729C>T, NM_001290104.1:c.702C>T, NM_001376233.1:c.702C>T

Select item 14857330705.

rs1485733070 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:21210188 (GRCh38)
16:21221509 (GRCh37)
Canonical SPDI:: NC_000016.10:21210187:A:G
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21210188A>G, NC_000016.9:g.21221509A>G, NW_017852933.1:g.33879A>G, NM_003460.2:c.156T>C, NM_003460.1:c.156T>C, NM_001376232.1:c.156T>C, NM_001290104.1:c.156T>C, NM_001376231.1:c.156T>C, NR_164788.1:n.183T>C, NM_001376233.1:c.156T>C

Select item 14847969056.

rs1484796905 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:21198824 (GRCh38)
16:21210145 (GRCh37)
Canonical SPDI:: NC_000016.10:21198823:G:A
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
HGVS:: NC_000016.10:g.21198824G>A, NC_000016.9:g.21210145G>A, NW_017852933.1:g.22515G>A, NM_003460.2:c.1966C>T, NM_003460.1:c.1966C>T, NM_001376232.1:c.1966C>T, NM_001290104.1:c.1939C>T, NM_001376231.1:c.1939C>T, NR_164788.1:n.1896C>T, NM_001376233.1:c.1999C>T, NP_003451.1:p.Leu656Phe, NP_001363161.1:p.Leu656Phe, NP_001363160.1:p.Leu647Phe, NP_001363162.1:p.Leu667Phe

Select item 14846830187.

rs1484683018 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:21201374 (GRCh38)
16:21212695 (GRCh37)
Canonical SPDI:: NC_000016.10:21201373:C:T
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000036/5 (GnomAD)
T=0.000042/11 (TOPMED)
HGVS:: NC_000016.10:g.21201374C>T, NC_000016.9:g.21212695C>T, NW_017852933.1:g.25065C>T, NM_003460.2:c.1689G>A, NM_003460.1:c.1689G>A, NM_001376232.1:c.1689G>A, NM_001376231.1:c.1662G>A, NR_164788.1:n.1716G>A, NM_001290104.1:c.1662G>A, NM_001376233.1:c.1689G>A

Select item 14825594448.

rs1482559444 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:21204343 (GRCh38)
16:21215664 (GRCh37)
Canonical SPDI:: NC_000016.10:21204342:T:A
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21204343T>A, NC_000016.9:g.21215664T>A, NW_017852933.1:g.28034T>A, NM_003460.2:c.755A>T, NM_003460.1:c.755A>T, NM_001376232.1:c.755A>T, NM_001376231.1:c.755A>T, NR_164788.1:n.782A>T, NM_001290104.1:c.755A>T, NM_001376233.1:c.755A>T, NP_003451.1:p.Lys252Met, NP_001363161.1:p.Lys252Met, NP_001363160.1:p.Lys252Met, NP_001363162.1:p.Lys252Met

Select item 14816466549.

rs1481646654 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:21197533 (GRCh38)
16:21208854 (GRCh37)
Canonical SPDI:: NC_000016.10:21197532:T:C
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21197533T>C, NC_000016.9:g.21208854T>C, NW_017852933.1:g.21224T>C, NM_003460.2:c.2185A>G, NM_003460.1:c.2185A>G, NM_001376232.1:c.2185A>G, NM_001290104.1:c.2158A>G, NM_001376231.1:c.2158A>G, NR_164788.1:n.2115A>G, NM_001376233.1:c.2218A>G, NP_003451.1:p.Thr729Ala, NP_001363161.1:p.Thr729Ala, NP_001363160.1:p.Thr720Ala, NP_001363162.1:p.Thr740Ala

Select item 147941951810.

rs1479419518 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:21199855 (GRCh38)
16:21211176 (GRCh37)
Canonical SPDI:: NC_000016.10:21199854:T:A
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.21199855T>A, NC_000016.9:g.21211176T>A, NW_017852933.1:g.23546T>A, NM_003460.2:c.1718A>T, NM_003460.1:c.1718A>T, NM_001376232.1:c.1718A>T, NM_001376231.1:c.1691A>T, NR_164788.1:n.1745A>T, NM_001290104.1:c.1691A>T, NM_001376233.1:c.1718A>T, NP_003451.1:p.Tyr573Phe, NP_001363161.1:p.Tyr573Phe, NP_001363160.1:p.Tyr564Phe, NP_001363162.1:p.Tyr573Phe

Select item 147729674411.

rs1477296744 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 16:21201782 (GRCh38)
16:21213103 (GRCh37)
Canonical SPDI:: NC_000016.10:21201781:G:
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000016.10:g.21201782del, NC_000016.9:g.21213103del, NW_017852933.1:g.25473del, NM_003460.2:c.1428del, NM_003460.1:c.1428del, NM_001376232.1:c.1428del, NM_001290104.1:c.1401del, NM_001376231.1:c.1401del, NR_164788.1:n.1455del, NM_001376233.1:c.1428del, NP_003451.1:p.Asn477fs, NP_001363161.1:p.Asn477fs, NP_001363160.1:p.Asn468fs, NP_001363162.1:p.Asn477fs

Select item 147084245412.

rs1470842454 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 16:21205525 (GRCh38)
16:21216846 (GRCh37)
Canonical SPDI:: NC_000016.10:21205524:A:T
Gene:: ZP2 (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 (TOPMED)
T=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21205525A>T, NC_000016.9:g.21216846A>T, NW_017852933.1:g.29216A>T, NM_003460.2:c.588T>A, NM_003460.1:c.588T>A, NM_001376232.1:c.588T>A, NM_001290104.1:c.588T>A, NM_001376231.1:c.588T>A, NR_164788.1:n.615T>A, NM_001376233.1:c.588T>A

Select item 146974838513.

rs1469748385 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:21199796 (GRCh38)
16:21211117 (GRCh37)
Canonical SPDI:: NC_000016.10:21199795:A:G
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000016.10:g.21199796A>G, NC_000016.9:g.21211117A>G, NW_017852933.1:g.23487A>G, NM_003460.2:c.1777T>C, NM_003460.1:c.1777T>C, NM_001376232.1:c.1777T>C, NM_001376231.1:c.1750T>C, NR_164788.1:n.1804T>C, NM_001290104.1:c.1750T>C, NM_001376233.1:c.1777T>C, NP_003451.1:p.Phe593Leu, NP_001363161.1:p.Phe593Leu, NP_001363160.1:p.Phe584Leu, NP_001363162.1:p.Phe593Leu

Select item 146921754014.

rs1469217540 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 16:21206846 (GRCh38)
16:21218167 (GRCh37)
Canonical SPDI:: NC_000016.10:21206845:A:T
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21206846A>T, NC_000016.9:g.21218167A>T, NW_017852933.1:g.30537A>T, NM_003460.2:c.475T>A, NM_003460.1:c.475T>A, NM_001376232.1:c.475T>A, NM_001290104.1:c.475T>A, NM_001376231.1:c.475T>A, NR_164788.1:n.502T>A, NM_001376233.1:c.475T>A, NP_003451.1:p.Phe159Ile, NP_001363161.1:p.Phe159Ile, NP_001363160.1:p.Phe159Ile, NP_001363162.1:p.Phe159Ile

Select item 146879696715.

rs1468796967 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:21201762 (GRCh38)
16:21213083 (GRCh37)
Canonical SPDI:: NC_000016.10:21201761:G:A
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000016.10:g.21201762G>A, NC_000016.9:g.21213083G>A, NW_017852933.1:g.25453G>A, NM_003460.2:c.1448C>T, NM_003460.1:c.1448C>T, NM_001376232.1:c.1448C>T, NM_001376231.1:c.1421C>T, NR_164788.1:n.1475C>T, NM_001290104.1:c.1421C>T, NM_001376233.1:c.1448C>T, NP_003451.1:p.Pro483Leu, NP_001363161.1:p.Pro483Leu, NP_001363160.1:p.Pro474Leu, NP_001363162.1:p.Pro483Leu

Select item 146789125016.

rs1467891250 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:21209723 (GRCh38)
16:21221044 (GRCh37)
Canonical SPDI:: NC_000016.10:21209722:G:C
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21209723G>C, NC_000016.9:g.21221044G>C, NW_017852933.1:g.33414G>C, NM_003460.2:c.238C>G, NM_003460.1:c.238C>G, NM_001376232.1:c.238C>G, NM_001290104.1:c.238C>G, NM_001376231.1:c.238C>G, NR_164788.1:n.265C>G, NM_001376233.1:c.238C>G, NP_003451.1:p.Pro80Ala, NP_001363161.1:p.Pro80Ala, NP_001363160.1:p.Pro80Ala, NP_001363162.1:p.Pro80Ala

Select item 146780090417.

rs1467800904 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:21197783 (GRCh38)
16:21209104 (GRCh37)
Canonical SPDI:: NC_000016.10:21197782:T:A
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000016.10:g.21197783T>A, NC_000016.9:g.21209104T>A, NW_017852933.1:g.21474T>A, NM_003460.2:c.2078A>T, NM_003460.1:c.2078A>T, NM_001376232.1:c.2078A>T, NM_001290104.1:c.2051A>T, NM_001376231.1:c.2051A>T, NR_164788.1:n.2008A>T, NM_001376233.1:c.2111A>T, NP_003451.1:p.Glu693Val, NP_001363161.1:p.Glu693Val, NP_001363160.1:p.Glu684Val, NP_001363162.1:p.Glu704Val

Select item 146773368218.

rs1467733682 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:21199793 (GRCh38)
16:21211114 (GRCh37)
Canonical SPDI:: NC_000016.10:21199792:C:G
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
HGVS:: NC_000016.10:g.21199793C>G, NC_000016.9:g.21211114C>G, NW_017852933.1:g.23484C>G, NM_003460.2:c.1780G>C, NM_003460.1:c.1780G>C, NM_001376232.1:c.1780G>C, NM_001376231.1:c.1753G>C, NR_164788.1:n.1807G>C, NM_001290104.1:c.1753G>C, NM_001376233.1:c.1780G>C, NP_003451.1:p.Asp594His, NP_001363161.1:p.Asp594His, NP_001363160.1:p.Asp585His, NP_001363162.1:p.Asp594His

Select item 146684970119.

rs1466849701 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:21206839 (GRCh38)
16:21218160 (GRCh37)
Canonical SPDI:: NC_000016.10:21206838:G:A
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.21206839G>A, NC_000016.9:g.21218160G>A, NW_017852933.1:g.30530G>A, NM_003460.2:c.482C>T, NM_003460.1:c.482C>T, NM_001376232.1:c.482C>T, NM_001290104.1:c.482C>T, NM_001376231.1:c.482C>T, NR_164788.1:n.509C>T, NM_001376233.1:c.482C>T, NP_003451.1:p.Ser161Phe, NP_001363161.1:p.Ser161Phe, NP_001363160.1:p.Ser161Phe, NP_001363162.1:p.Ser161Phe

Select item 146682114320.

rs1466821143 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 16:21202023 (GRCh38)
16:21213344 (GRCh37)
Canonical SPDI:: NC_000016.10:21202022:A:T
Gene:: ZP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.21202023A>T, NC_000016.9:g.21213344A>T, NW_017852933.1:g.25714A>T, NM_003460.2:c.1288T>A, NM_003460.1:c.1288T>A, NM_001376232.1:c.1288T>A, NM_001290104.1:c.1288T>A, NM_001376231.1:c.1288T>A, NR_164788.1:n.1315T>A, NM_001376233.1:c.1288T>A, NP_003451.1:p.Phe430Ile, NP_001363161.1:p.Phe430Ile, NP_001363160.1:p.Phe430Ile, NP_001363162.1:p.Phe430Ile

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