SNP Links for Protein (Select 481026555) - SNP

Links from Protein

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Select item 14907734461.

rs1490773446 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:63186746 (GRCh38)
8:64099304 (GRCh37)
Canonical SPDI:: NC_000008.11:63186745:T:G
Gene:: YTHDF3 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000056/2 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.63186746T>G, NC_000008.10:g.64099304T>G, NG_033226.1:g.23194T>G, NM_152758.6:c.735T>G, NM_152758.5:c.735T>G, NM_001277813.2:c.744T>G, NM_001277813.1:c.744T>G, NM_001277815.2:c.582T>G, NM_001277815.1:c.582T>G, NM_001277814.2:c.744T>G, NM_001277814.1:c.744T>G, NM_001277816.2:c.582T>G, NM_001277816.1:c.582T>G, NM_001277817.2:c.582T>G, NM_001277817.1:c.582T>G, NM_001277818.2:c.582T>G, NM_001277818.1:c.582T>G, XM_011517509.4:c.744T>G, XM_011517509.3:c.744T>G, XM_011517509.2:c.744T>G, XM_011517509.1:c.744T>G, XM_011517510.4:c.582T>G, XM_011517510.3:c.582T>G, XM_011517510.2:c.582T>G, XM_011517510.1:c.582T>G

Select item 14897823072.

rs1489782307 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:63187663 (GRCh38)
8:64100221 (GRCh37)
Canonical SPDI:: NC_000008.11:63187662:C:G
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.63187663C>G, NC_000008.10:g.64100221C>G, NG_033226.1:g.24111C>G, NM_152758.6:c.1652C>G, NM_152758.5:c.1652C>G, NM_001277813.2:c.1661C>G, NM_001277813.1:c.1661C>G, NM_001277815.2:c.1499C>G, NM_001277815.1:c.1499C>G, NM_001277814.2:c.1661C>G, NM_001277814.1:c.1661C>G, NM_001277816.2:c.1499C>G, NM_001277816.1:c.1499C>G, NM_001277817.2:c.1499C>G, NM_001277817.1:c.1499C>G, NM_001277818.2:c.1499C>G, NM_001277818.1:c.1499C>G, XM_011517509.4:c.1661C>G, XM_011517509.3:c.1661C>G, XM_011517509.2:c.1661C>G, XM_011517509.1:c.1661C>G, XM_011517510.4:c.1499C>G, XM_011517510.3:c.1499C>G, XM_011517510.2:c.1499C>G, XM_011517510.1:c.1499C>G, NP_689971.4:p.Ala551Gly, NP_001264742.1:p.Ala554Gly, NP_001264744.1:p.Ala500Gly, NP_001264743.1:p.Ala554Gly, NP_001264745.1:p.Ala500Gly, NP_001264746.1:p.Ala500Gly, NP_001264747.1:p.Ala500Gly, XP_011515811.1:p.Ala554Gly, XP_011515812.1:p.Ala500Gly

Select item 14888977243.

rs1488897724 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:63186266 (GRCh38)
8:64098824 (GRCh37)
Canonical SPDI:: NC_000008.11:63186265:A:G
Gene:: YTHDF3 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.63186266A>G, NC_000008.10:g.64098824A>G, NG_033226.1:g.22714A>G, NM_152758.6:c.255A>G, NM_152758.5:c.255A>G, NM_001277813.2:c.264A>G, NM_001277813.1:c.264A>G, NM_001277815.2:c.102A>G, NM_001277815.1:c.102A>G, NM_001277814.2:c.264A>G, NM_001277814.1:c.264A>G, NM_001277816.2:c.102A>G, NM_001277816.1:c.102A>G, NM_001277817.2:c.102A>G, NM_001277817.1:c.102A>G, NM_001277818.2:c.102A>G, NM_001277818.1:c.102A>G, XM_011517509.4:c.264A>G, XM_011517509.3:c.264A>G, XM_011517509.2:c.264A>G, XM_011517509.1:c.264A>G, XM_011517510.4:c.102A>G, XM_011517510.3:c.102A>G, XM_011517510.2:c.102A>G, XM_011517510.1:c.102A>G

Select item 14880494244.

rs1488049424 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:63172774 (GRCh38)
8:64085333 (GRCh37)
Canonical SPDI:: NC_000008.11:63172773:G:A
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000066/1 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000008.11:g.63172774G>A, NC_000008.10:g.64085333G>A, NG_033226.1:g.9222G>A, NM_001277813.2:c.34G>A, NM_001277813.1:c.34G>A, NM_001277814.2:c.34G>A, NM_001277814.1:c.34G>A, XM_011517509.4:c.34G>A, XM_011517509.3:c.34G>A, XM_011517509.2:c.34G>A, XM_011517509.1:c.34G>A, NP_001264742.1:p.Ala12Thr, NP_001264743.1:p.Ala12Thr, XP_011515811.1:p.Ala12Thr

Select item 14875564925.

rs1487556492 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:63186711 (GRCh38)
8:64099269 (GRCh37)
Canonical SPDI:: NC_000008.11:63186710:A:G
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_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_000008.11:g.63186711A>G, NC_000008.10:g.64099269A>G, NG_033226.1:g.23159A>G, NM_152758.6:c.700A>G, NM_152758.5:c.700A>G, NM_001277813.2:c.709A>G, NM_001277813.1:c.709A>G, NM_001277815.2:c.547A>G, NM_001277815.1:c.547A>G, NM_001277814.2:c.709A>G, NM_001277814.1:c.709A>G, NM_001277816.2:c.547A>G, NM_001277816.1:c.547A>G, NM_001277817.2:c.547A>G, NM_001277817.1:c.547A>G, NM_001277818.2:c.547A>G, NM_001277818.1:c.547A>G, XM_011517509.4:c.709A>G, XM_011517509.3:c.709A>G, XM_011517509.2:c.709A>G, XM_011517509.1:c.709A>G, XM_011517510.4:c.547A>G, XM_011517510.3:c.547A>G, XM_011517510.2:c.547A>G, XM_011517510.1:c.547A>G, NP_689971.4:p.Lys234Glu, NP_001264742.1:p.Lys237Glu, NP_001264744.1:p.Lys183Glu, NP_001264743.1:p.Lys237Glu, NP_001264745.1:p.Lys183Glu, NP_001264746.1:p.Lys183Glu, NP_001264747.1:p.Lys183Glu, XP_011515811.1:p.Lys237Glu, XP_011515812.1:p.Lys183Glu

Select item 14856000046.

rs1485600004 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:63187547 (GRCh38)
8:64100105 (GRCh37)
Canonical SPDI:: NC_000008.11:63187546:C:T
Gene:: YTHDF3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_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_000008.11:g.63187547C>T, NC_000008.10:g.64100105C>T, NG_033226.1:g.23995C>T, NM_152758.6:c.1536C>T, NM_152758.5:c.1536C>T, NM_001277813.2:c.1545C>T, NM_001277813.1:c.1545C>T, NM_001277815.2:c.1383C>T, NM_001277815.1:c.1383C>T, NM_001277814.2:c.1545C>T, NM_001277814.1:c.1545C>T, NM_001277816.2:c.1383C>T, NM_001277816.1:c.1383C>T, NM_001277817.2:c.1383C>T, NM_001277817.1:c.1383C>T, NM_001277818.2:c.1383C>T, NM_001277818.1:c.1383C>T, XM_011517509.4:c.1545C>T, XM_011517509.3:c.1545C>T, XM_011517509.2:c.1545C>T, XM_011517509.1:c.1545C>T, XM_011517510.4:c.1383C>T, XM_011517510.3:c.1383C>T, XM_011517510.2:c.1383C>T, XM_011517510.1:c.1383C>T

Select item 14831100327.

rs1483110032 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:63186864 (GRCh38)
8:64099422 (GRCh37)
Canonical SPDI:: NC_000008.11:63186863:G:C
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.63186864G>C, NC_000008.10:g.64099422G>C, NG_033226.1:g.23312G>C, NM_152758.6:c.853G>C, NM_152758.5:c.853G>C, NM_001277813.2:c.862G>C, NM_001277813.1:c.862G>C, NM_001277815.2:c.700G>C, NM_001277815.1:c.700G>C, NM_001277814.2:c.862G>C, NM_001277814.1:c.862G>C, NM_001277816.2:c.700G>C, NM_001277816.1:c.700G>C, NM_001277817.2:c.700G>C, NM_001277817.1:c.700G>C, NM_001277818.2:c.700G>C, NM_001277818.1:c.700G>C, XM_011517509.4:c.862G>C, XM_011517509.3:c.862G>C, XM_011517509.2:c.862G>C, XM_011517509.1:c.862G>C, XM_011517510.4:c.700G>C, XM_011517510.3:c.700G>C, XM_011517510.2:c.700G>C, XM_011517510.1:c.700G>C, NP_689971.4:p.Val285Leu, NP_001264742.1:p.Val288Leu, NP_001264744.1:p.Val234Leu, NP_001264743.1:p.Val288Leu, NP_001264745.1:p.Val234Leu, NP_001264746.1:p.Val234Leu, NP_001264747.1:p.Val234Leu, XP_011515811.1:p.Val288Leu, XP_011515812.1:p.Val234Leu

Select item 14829187558.

rs1482918755 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:63186316 (GRCh38)
8:64098874 (GRCh37)
Canonical SPDI:: NC_000008.11:63186315:C:T
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.63186316C>T, NC_000008.10:g.64098874C>T, NG_033226.1:g.22764C>T, NM_152758.6:c.305C>T, NM_152758.5:c.305C>T, NM_001277813.2:c.314C>T, NM_001277813.1:c.314C>T, NM_001277815.2:c.152C>T, NM_001277815.1:c.152C>T, NM_001277814.2:c.314C>T, NM_001277814.1:c.314C>T, NM_001277816.2:c.152C>T, NM_001277816.1:c.152C>T, NM_001277817.2:c.152C>T, NM_001277817.1:c.152C>T, NM_001277818.2:c.152C>T, NM_001277818.1:c.152C>T, XM_011517509.4:c.314C>T, XM_011517509.3:c.314C>T, XM_011517509.2:c.314C>T, XM_011517509.1:c.314C>T, XM_011517510.4:c.152C>T, XM_011517510.3:c.152C>T, XM_011517510.2:c.152C>T, XM_011517510.1:c.152C>T, NP_689971.4:p.Pro102Leu, NP_001264742.1:p.Pro105Leu, NP_001264744.1:p.Pro51Leu, NP_001264743.1:p.Pro105Leu, NP_001264745.1:p.Pro51Leu, NP_001264746.1:p.Pro51Leu, NP_001264747.1:p.Pro51Leu, XP_011515811.1:p.Pro105Leu, XP_011515812.1:p.Pro51Leu

Select item 14765758639.

rs1476575863 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 8:63187023 (GRCh38)
8:64099581 (GRCh37)
Canonical SPDI:: NC_000008.11:63187022:G:C,NC_000008.11:63187022:G:T
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
T=0.000035/1 (TOMMO)
HGVS:: NC_000008.11:g.63187023G>C, NC_000008.11:g.63187023G>T, NC_000008.10:g.64099581G>C, NC_000008.10:g.64099581G>T, NG_033226.1:g.23471G>C, NG_033226.1:g.23471G>T, NM_152758.6:c.1012G>C, NM_152758.6:c.1012G>T, NM_152758.5:c.1012G>C, NM_152758.5:c.1012G>T, NM_001277813.2:c.1021G>C, NM_001277813.2:c.1021G>T, NM_001277813.1:c.1021G>C, NM_001277813.1:c.1021G>T, NM_001277815.2:c.859G>C, NM_001277815.2:c.859G>T, NM_001277815.1:c.859G>C, NM_001277815.1:c.859G>T, NM_001277814.2:c.1021G>C, NM_001277814.2:c.1021G>T, NM_001277814.1:c.1021G>C, NM_001277814.1:c.1021G>T, NM_001277816.2:c.859G>C, NM_001277816.2:c.859G>T, NM_001277816.1:c.859G>C, NM_001277816.1:c.859G>T, NM_001277817.2:c.859G>C, NM_001277817.2:c.859G>T, NM_001277817.1:c.859G>C, NM_001277817.1:c.859G>T, NM_001277818.2:c.859G>C, NM_001277818.2:c.859G>T, NM_001277818.1:c.859G>C, NM_001277818.1:c.859G>T, XM_011517509.4:c.1021G>C, XM_011517509.4:c.1021G>T, XM_011517509.3:c.1021G>C, XM_011517509.3:c.1021G>T, XM_011517509.2:c.1021G>C, XM_011517509.2:c.1021G>T, XM_011517509.1:c.1021G>C, XM_011517509.1:c.1021G>T, XM_011517510.4:c.859G>C, XM_011517510.4:c.859G>T, XM_011517510.3:c.859G>C, XM_011517510.3:c.859G>T, XM_011517510.2:c.859G>C, XM_011517510.2:c.859G>T, XM_011517510.1:c.859G>C, XM_011517510.1:c.859G>T, NP_689971.4:p.Ala338Pro, NP_689971.4:p.Ala338Ser, NP_001264742.1:p.Ala341Pro, NP_001264742.1:p.Ala341Ser, NP_001264744.1:p.Ala287Pro, NP_001264744.1:p.Ala287Ser, NP_001264743.1:p.Ala341Pro, NP_001264743.1:p.Ala341Ser, NP_001264745.1:p.Ala287Pro, NP_001264745.1:p.Ala287Ser, NP_001264746.1:p.Ala287Pro, NP_001264746.1:p.Ala287Ser, NP_001264747.1:p.Ala287Pro, NP_001264747.1:p.Ala287Ser, XP_011515811.1:p.Ala341Pro, XP_011515811.1:p.Ala341Ser, XP_011515812.1:p.Ala287Pro, XP_011515812.1:p.Ala287Ser

Select item 147250531610.

rs1472505316 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 8:63186180 (GRCh38)
8:64098738 (GRCh37)
Canonical SPDI:: NC_000008.11:63186179:A:G,NC_000008.11:63186179:A:T
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000047/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.63186180A>G, NC_000008.11:g.63186180A>T, NC_000008.10:g.64098738A>G, NC_000008.10:g.64098738A>T, NG_033226.1:g.22628A>G, NG_033226.1:g.22628A>T, NM_152758.6:c.169A>G, NM_152758.6:c.169A>T, NM_152758.5:c.169A>G, NM_152758.5:c.169A>T, NM_001277813.2:c.178A>G, NM_001277813.2:c.178A>T, NM_001277813.1:c.178A>G, NM_001277813.1:c.178A>T, NM_001277815.2:c.16A>G, NM_001277815.2:c.16A>T, NM_001277815.1:c.16A>G, NM_001277815.1:c.16A>T, NM_001277814.2:c.178A>G, NM_001277814.2:c.178A>T, NM_001277814.1:c.178A>G, NM_001277814.1:c.178A>T, NM_001277816.2:c.16A>G, NM_001277816.2:c.16A>T, NM_001277816.1:c.16A>G, NM_001277816.1:c.16A>T, NM_001277817.2:c.16A>G, NM_001277817.2:c.16A>T, NM_001277817.1:c.16A>G, NM_001277817.1:c.16A>T, NM_001277818.2:c.16A>G, NM_001277818.2:c.16A>T, NM_001277818.1:c.16A>G, NM_001277818.1:c.16A>T, XM_011517509.4:c.178A>G, XM_011517509.4:c.178A>T, XM_011517509.3:c.178A>G, XM_011517509.3:c.178A>T, XM_011517509.2:c.178A>G, XM_011517509.2:c.178A>T, XM_011517509.1:c.178A>G, XM_011517509.1:c.178A>T, XM_011517510.4:c.16A>G, XM_011517510.4:c.16A>T, XM_011517510.3:c.16A>G, XM_011517510.3:c.16A>T, XM_011517510.2:c.16A>G, XM_011517510.2:c.16A>T, XM_011517510.1:c.16A>G, XM_011517510.1:c.16A>T, NP_689971.4:p.Met57Val, NP_689971.4:p.Met57Leu, NP_001264742.1:p.Met60Val, NP_001264742.1:p.Met60Leu, NP_001264744.1:p.Met6Val, NP_001264744.1:p.Met6Leu, NP_001264743.1:p.Met60Val, NP_001264743.1:p.Met60Leu, NP_001264745.1:p.Met6Val, NP_001264745.1:p.Met6Leu, NP_001264746.1:p.Met6Val, NP_001264746.1:p.Met6Leu, NP_001264747.1:p.Met6Val, NP_001264747.1:p.Met6Leu, XP_011515811.1:p.Met60Val, XP_011515811.1:p.Met60Leu, XP_011515812.1:p.Met6Val, XP_011515812.1:p.Met6Leu

Select item 147048486311.

rs1470484863 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:63186760 (GRCh38)
8:64099318 (GRCh37)
Canonical SPDI:: NC_000008.11:63186759:C:T
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.63186760C>T, NC_000008.10:g.64099318C>T, NG_033226.1:g.23208C>T, NM_152758.6:c.749C>T, NM_152758.5:c.749C>T, NM_001277813.2:c.758C>T, NM_001277813.1:c.758C>T, NM_001277815.2:c.596C>T, NM_001277815.1:c.596C>T, NM_001277814.2:c.758C>T, NM_001277814.1:c.758C>T, NM_001277816.2:c.596C>T, NM_001277816.1:c.596C>T, NM_001277817.2:c.596C>T, NM_001277817.1:c.596C>T, NM_001277818.2:c.596C>T, NM_001277818.1:c.596C>T, XM_011517509.4:c.758C>T, XM_011517509.3:c.758C>T, XM_011517509.2:c.758C>T, XM_011517509.1:c.758C>T, XM_011517510.4:c.596C>T, XM_011517510.3:c.596C>T, XM_011517510.2:c.596C>T, XM_011517510.1:c.596C>T, NP_689971.4:p.Pro250Leu, NP_001264742.1:p.Pro253Leu, NP_001264744.1:p.Pro199Leu, NP_001264743.1:p.Pro253Leu, NP_001264745.1:p.Pro199Leu, NP_001264746.1:p.Pro199Leu, NP_001264747.1:p.Pro199Leu, XP_011515811.1:p.Pro253Leu, XP_011515812.1:p.Pro199Leu

Select item 146985990112.

rs1469859901 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:63186173 (GRCh38)
8:64098731 (GRCh37)
Canonical SPDI:: NC_000008.11:63186172:T:C
Gene:: YTHDF3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.63186173T>C, NC_000008.10:g.64098731T>C, NG_033226.1:g.22621T>C, NM_152758.6:c.162T>C, NM_152758.5:c.162T>C, NM_001277813.2:c.171T>C, NM_001277813.1:c.171T>C, NM_001277815.2:c.9T>C, NM_001277815.1:c.9T>C, NM_001277814.2:c.171T>C, NM_001277814.1:c.171T>C, NM_001277816.2:c.9T>C, NM_001277816.1:c.9T>C, NM_001277817.2:c.9T>C, NM_001277817.1:c.9T>C, NM_001277818.2:c.9T>C, NM_001277818.1:c.9T>C, XM_011517509.4:c.171T>C, XM_011517509.3:c.171T>C, XM_011517509.2:c.171T>C, XM_011517509.1:c.171T>C, XM_011517510.4:c.9T>C, XM_011517510.3:c.9T>C, XM_011517510.2:c.9T>C, XM_011517510.1:c.9T>C

Select item 146441911913.

rs1464419119 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 8:63186894 (GRCh38)
8:64099452 (GRCh37)
Canonical SPDI:: NC_000008.11:63186893:C:A,NC_000008.11:63186893:C:G
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000008.11:g.63186894C>A, NC_000008.11:g.63186894C>G, NC_000008.10:g.64099452C>A, NC_000008.10:g.64099452C>G, NG_033226.1:g.23342C>A, NG_033226.1:g.23342C>G, NM_152758.6:c.883C>A, NM_152758.6:c.883C>G, NM_152758.5:c.883C>A, NM_152758.5:c.883C>G, NM_001277813.2:c.892C>A, NM_001277813.2:c.892C>G, NM_001277813.1:c.892C>A, NM_001277813.1:c.892C>G, NM_001277815.2:c.730C>A, NM_001277815.2:c.730C>G, NM_001277815.1:c.730C>A, NM_001277815.1:c.730C>G, NM_001277814.2:c.892C>A, NM_001277814.2:c.892C>G, NM_001277814.1:c.892C>A, NM_001277814.1:c.892C>G, NM_001277816.2:c.730C>A, NM_001277816.2:c.730C>G, NM_001277816.1:c.730C>A, NM_001277816.1:c.730C>G, NM_001277817.2:c.730C>A, NM_001277817.2:c.730C>G, NM_001277817.1:c.730C>A, NM_001277817.1:c.730C>G, NM_001277818.2:c.730C>A, NM_001277818.2:c.730C>G, NM_001277818.1:c.730C>A, NM_001277818.1:c.730C>G, XM_011517509.4:c.892C>A, XM_011517509.4:c.892C>G, XM_011517509.3:c.892C>A, XM_011517509.3:c.892C>G, XM_011517509.2:c.892C>A, XM_011517509.2:c.892C>G, XM_011517509.1:c.892C>A, XM_011517509.1:c.892C>G, XM_011517510.4:c.730C>A, XM_011517510.4:c.730C>G, XM_011517510.3:c.730C>A, XM_011517510.3:c.730C>G, XM_011517510.2:c.730C>A, XM_011517510.2:c.730C>G, XM_011517510.1:c.730C>A, XM_011517510.1:c.730C>G, NP_689971.4:p.Leu295Met, NP_689971.4:p.Leu295Val, NP_001264742.1:p.Leu298Met, NP_001264742.1:p.Leu298Val, NP_001264744.1:p.Leu244Met, NP_001264744.1:p.Leu244Val, NP_001264743.1:p.Leu298Met, NP_001264743.1:p.Leu298Val, NP_001264745.1:p.Leu244Met, NP_001264745.1:p.Leu244Val, NP_001264746.1:p.Leu244Met, NP_001264746.1:p.Leu244Val, NP_001264747.1:p.Leu244Met, NP_001264747.1:p.Leu244Val, XP_011515811.1:p.Leu298Met, XP_011515811.1:p.Leu298Val, XP_011515812.1:p.Leu244Met, XP_011515812.1:p.Leu244Val

Select item 146374404314.

rs1463744043 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 8:63175345 (GRCh38)
8:64087904 (GRCh37)
Canonical SPDI:: NC_000008.11:63175344:G:A,NC_000008.11:63175344:G:C
Gene:: YTHDF3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,5_prime_UTR_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.63175345G>A, NC_000008.11:g.63175345G>C, NC_000008.10:g.64087904G>A, NC_000008.10:g.64087904G>C, NG_033226.1:g.11793G>A, NG_033226.1:g.11793G>C, NM_152758.6:c.64G>A, NM_152758.6:c.64G>C, NM_152758.5:c.64G>A, NM_152758.5:c.64G>C, NM_001277813.2:c.73G>A, NM_001277813.2:c.73G>C, NM_001277813.1:c.73G>A, NM_001277813.1:c.73G>C, NM_001277815.2:c.-90G>A, NM_001277815.2:c.-90G>C, NM_001277815.1:c.-90G>A, NM_001277815.1:c.-90G>C, NM_001277814.2:c.73G>A, NM_001277814.2:c.73G>C, NM_001277814.1:c.73G>A, NM_001277814.1:c.73G>C, NM_001277817.2:c.-90G>A, NM_001277817.2:c.-90G>C, NM_001277817.1:c.-90G>A, NM_001277817.1:c.-90G>C, NM_001277818.2:c.-90G>A, NM_001277818.2:c.-90G>C, NM_001277818.1:c.-90G>A, NM_001277818.1:c.-90G>C, NR_102434.1:n.389G>A, NR_102434.1:n.389G>C, XM_011517509.4:c.73G>A, XM_011517509.4:c.73G>C, XM_011517509.3:c.73G>A, XM_011517509.3:c.73G>C, XM_011517509.2:c.73G>A, XM_011517509.2:c.73G>C, XM_011517509.1:c.73G>A, XM_011517509.1:c.73G>C, NP_689971.4:p.Gly22Ser, NP_689971.4:p.Gly22Arg, NP_001264742.1:p.Gly25Ser, NP_001264742.1:p.Gly25Arg, NP_001264743.1:p.Gly25Ser, NP_001264743.1:p.Gly25Arg, XP_011515811.1:p.Gly25Ser, XP_011515811.1:p.Gly25Arg

Select item 146083218615.

rs1460832186 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:63187001 (GRCh38)
8:64099559 (GRCh37)
Canonical SPDI:: NC_000008.11:63187000:G:A
Gene:: YTHDF3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
HGVS:: NC_000008.11:g.63187001G>A, NC_000008.10:g.64099559G>A, NG_033226.1:g.23449G>A, NM_152758.6:c.990G>A, NM_152758.5:c.990G>A, NM_001277813.2:c.999G>A, NM_001277813.1:c.999G>A, NM_001277815.2:c.837G>A, NM_001277815.1:c.837G>A, NM_001277814.2:c.999G>A, NM_001277814.1:c.999G>A, NM_001277816.2:c.837G>A, NM_001277816.1:c.837G>A, NM_001277817.2:c.837G>A, NM_001277817.1:c.837G>A, NM_001277818.2:c.837G>A, NM_001277818.1:c.837G>A, XM_011517509.4:c.999G>A, XM_011517509.3:c.999G>A, XM_011517509.2:c.999G>A, XM_011517509.1:c.999G>A, XM_011517510.4:c.837G>A, XM_011517510.3:c.837G>A, XM_011517510.2:c.837G>A, XM_011517510.1:c.837G>A

Select item 146038925016.

rs1460389250 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:63187401 (GRCh38)
8:64099959 (GRCh37)
Canonical SPDI:: NC_000008.11:63187400:C:T
Gene:: YTHDF3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.63187401C>T, NC_000008.10:g.64099959C>T, NG_033226.1:g.23849C>T, NM_152758.6:c.1390C>T, NM_152758.5:c.1390C>T, NM_001277813.2:c.1399C>T, NM_001277813.1:c.1399C>T, NM_001277815.2:c.1237C>T, NM_001277815.1:c.1237C>T, NM_001277814.2:c.1399C>T, NM_001277814.1:c.1399C>T, NM_001277816.2:c.1237C>T, NM_001277816.1:c.1237C>T, NM_001277817.2:c.1237C>T, NM_001277817.1:c.1237C>T, NM_001277818.2:c.1237C>T, NM_001277818.1:c.1237C>T, XM_011517509.4:c.1399C>T, XM_011517509.3:c.1399C>T, XM_011517509.2:c.1399C>T, XM_011517509.1:c.1399C>T, XM_011517510.4:c.1237C>T, XM_011517510.3:c.1237C>T, XM_011517510.2:c.1237C>T, XM_011517510.1:c.1237C>T, NP_689971.4:p.Leu464Phe, NP_001264742.1:p.Leu467Phe, NP_001264744.1:p.Leu413Phe, NP_001264743.1:p.Leu467Phe, NP_001264745.1:p.Leu413Phe, NP_001264746.1:p.Leu413Phe, NP_001264747.1:p.Leu413Phe, XP_011515811.1:p.Leu467Phe, XP_011515812.1:p.Leu413Phe

Select item 145566214617.

rs1455662146 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:63186378 (GRCh38)
8:64098936 (GRCh37)
Canonical SPDI:: NC_000008.11:63186377:G:A
Gene:: YTHDF3 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.63186378G>A, NC_000008.10:g.64098936G>A, NG_033226.1:g.22826G>A, NM_152758.6:c.367G>A, NM_152758.5:c.367G>A, NM_001277813.2:c.376G>A, NM_001277813.1:c.376G>A, NM_001277815.2:c.214G>A, NM_001277815.1:c.214G>A, NM_001277814.2:c.376G>A, NM_001277814.1:c.376G>A, NM_001277816.2:c.214G>A, NM_001277816.1:c.214G>A, NM_001277817.2:c.214G>A, NM_001277817.1:c.214G>A, NM_001277818.2:c.214G>A, NM_001277818.1:c.214G>A, XM_011517509.4:c.376G>A, XM_011517509.3:c.376G>A, XM_011517509.2:c.376G>A, XM_011517509.1:c.376G>A, XM_011517510.4:c.214G>A, XM_011517510.3:c.214G>A, XM_011517510.2:c.214G>A, XM_011517510.1:c.214G>A, NP_689971.4:p.Gly123Arg, NP_001264742.1:p.Gly126Arg, NP_001264744.1:p.Gly72Arg, NP_001264743.1:p.Gly126Arg, NP_001264745.1:p.Gly72Arg, NP_001264746.1:p.Gly72Arg, NP_001264747.1:p.Gly72Arg, XP_011515811.1:p.Gly126Arg, XP_011515812.1:p.Gly72Arg

Select item 145486441518.

rs1454864415 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 8:63186187 (GRCh38)
8:64098745 (GRCh37)
Canonical SPDI:: NC_000008.11:63186186:GT:
Gene:: YTHDF3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.63186187_63186188del, NC_000008.10:g.64098745_64098746del, NG_033226.1:g.22635_22636del, NM_152758.6:c.176_177del, NM_152758.5:c.176_177del, NM_001277813.2:c.185_186del, NM_001277813.1:c.185_186del, NM_001277815.2:c.23_24del, NM_001277815.1:c.23_24del, NM_001277814.2:c.185_186del, NM_001277814.1:c.185_186del, NM_001277816.2:c.23_24del, NM_001277816.1:c.23_24del, NM_001277817.2:c.23_24del, NM_001277817.1:c.23_24del, NM_001277818.2:c.23_24del, NM_001277818.1:c.23_24del, XM_011517509.4:c.185_186del, XM_011517509.3:c.185_186del, XM_011517509.2:c.185_186del, XM_011517509.1:c.185_186del, XM_011517510.4:c.23_24del, XM_011517510.3:c.23_24del, XM_011517510.2:c.23_24del, XM_011517510.1:c.23_24del, NP_689971.4:p.Ser59fs, NP_001264742.1:p.Ser62fs, NP_001264744.1:p.Ser8fs, NP_001264743.1:p.Ser62fs, NP_001264745.1:p.Ser8fs, NP_001264746.1:p.Ser8fs, NP_001264747.1:p.Ser8fs, XP_011515811.1:p.Ser62fs, XP_011515812.1:p.Ser8fs

Select item 145469069219.

rs1454690692 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:63187474 (GRCh38)
8:64100032 (GRCh37)
Canonical SPDI:: NC_000008.11:63187473:A:G
Gene:: YTHDF3 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.63187474A>G, NC_000008.10:g.64100032A>G, NG_033226.1:g.23922A>G, NM_152758.6:c.1463A>G, NM_152758.5:c.1463A>G, NM_001277813.2:c.1472A>G, NM_001277813.1:c.1472A>G, NM_001277815.2:c.1310A>G, NM_001277815.1:c.1310A>G, NM_001277814.2:c.1472A>G, NM_001277814.1:c.1472A>G, NM_001277816.2:c.1310A>G, NM_001277816.1:c.1310A>G, NM_001277817.2:c.1310A>G, NM_001277817.1:c.1310A>G, NM_001277818.2:c.1310A>G, NM_001277818.1:c.1310A>G, XM_011517509.4:c.1472A>G, XM_011517509.3:c.1472A>G, XM_011517509.2:c.1472A>G, XM_011517509.1:c.1472A>G, XM_011517510.4:c.1310A>G, XM_011517510.3:c.1310A>G, XM_011517510.2:c.1310A>G, XM_011517510.1:c.1310A>G, NP_689971.4:p.Tyr488Cys, NP_001264742.1:p.Tyr491Cys, NP_001264744.1:p.Tyr437Cys, NP_001264743.1:p.Tyr491Cys, NP_001264745.1:p.Tyr437Cys, NP_001264746.1:p.Tyr437Cys, NP_001264747.1:p.Tyr437Cys, XP_011515811.1:p.Tyr491Cys, XP_011515812.1:p.Tyr437Cys

Select item 145460661920.

rs1454606619 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:63186522 (GRCh38)
8:64099080 (GRCh37)
Canonical SPDI:: NC_000008.11:63186521:G:A
Gene:: YTHDF3 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.63186522G>A, NC_000008.10:g.64099080G>A, NG_033226.1:g.22970G>A, NM_152758.6:c.511G>A, NM_152758.5:c.511G>A, NM_001277813.2:c.520G>A, NM_001277813.1:c.520G>A, NM_001277815.2:c.358G>A, NM_001277815.1:c.358G>A, NM_001277814.2:c.520G>A, NM_001277814.1:c.520G>A, NM_001277816.2:c.358G>A, NM_001277816.1:c.358G>A, NM_001277817.2:c.358G>A, NM_001277817.1:c.358G>A, NM_001277818.2:c.358G>A, NM_001277818.1:c.358G>A, XM_011517509.4:c.520G>A, XM_011517509.3:c.520G>A, XM_011517509.2:c.520G>A, XM_011517509.1:c.520G>A, XM_011517510.4:c.358G>A, XM_011517510.3:c.358G>A, XM_011517510.2:c.358G>A, XM_011517510.1:c.358G>A, NP_689971.4:p.Ala171Thr, NP_001264742.1:p.Ala174Thr, NP_001264744.1:p.Ala120Thr, NP_001264743.1:p.Ala174Thr, NP_001264745.1:p.Ala120Thr, NP_001264746.1:p.Ala120Thr, NP_001264747.1:p.Ala120Thr, XP_011515811.1:p.Ala174Thr, XP_011515812.1:p.Ala120Thr

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