SNP Links for Nucleotide (Select 983173836) - SNP - NCBI

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Links from Nucleotide

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Select item 14875710241.

rs1487571024 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:63555985 (GRCh38)
20:62187338 (GRCh37)
Canonical SPDI:: NC_000020.11:63555984:T:C
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000020.11:g.63555985T>C, NC_000020.10:g.62187338T>C, XM_011529041.3:c.322T>C, XM_011529041.2:c.322T>C, XM_011529041.1:c.322T>C, NM_024059.3:c.322T>C, NM_024059.2:c.322T>C, XM_017028060.2:c.337T>C, XM_017028060.1:c.337T>C, NM_001319153.2:c.322T>C, NM_001319153.1:c.322T>C, NM_001319152.2:c.322T>C, NM_001319152.1:c.322T>C, XM_047440467.1:c.391T>C, XM_047440468.1:c.322T>C, XM_047440466.1:c.544T>C, XP_011527343.1:p.Phe108Leu, NP_076964.1:p.Phe108Leu, XP_016883549.1:p.Phe113Leu, NP_001306082.1:p.Phe108Leu, NP_001306081.1:p.Phe108Leu, XP_047296423.1:p.Phe131Leu, XP_047296424.1:p.Phe108Leu, XP_047296422.1:p.Phe182Leu

Select item 14841697592.

rs1484169759 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63555996 (GRCh38)
20:62187349 (GRCh37)
Canonical SPDI:: NC_000020.11:63555995:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63555996G>A, NC_000020.10:g.62187349G>A, XM_011529041.3:c.333G>A, XM_011529041.2:c.333G>A, XM_011529041.1:c.333G>A, NM_024059.3:c.333G>A, NM_024059.2:c.333G>A, XM_017028060.2:c.348G>A, XM_017028060.1:c.348G>A, NM_001319153.2:c.333G>A, NM_001319153.1:c.333G>A, NM_001319152.2:c.333G>A, NM_001319152.1:c.333G>A, XM_047440467.1:c.402G>A, XM_047440468.1:c.333G>A, XM_047440466.1:c.555G>A, XP_011527343.1:p.Met111Ile, NP_076964.1:p.Met111Ile, XP_016883549.1:p.Met116Ile, NP_001306082.1:p.Met111Ile, NP_001306081.1:p.Met111Ile, XP_047296423.1:p.Met134Ile, XP_047296424.1:p.Met111Ile, XP_047296422.1:p.Met185Ile

Select item 14825530923.

rs1482553092 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63556230 (GRCh38)
20:62187583 (GRCh37)
Canonical SPDI:: NC_000020.11:63556229:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63556230G>A, NC_000020.10:g.62187583G>A, XM_011529041.3:c.567G>A, XM_011529041.2:c.567G>A, XM_011529041.1:c.567G>A, NM_024059.3:c.567G>A, NM_024059.2:c.567G>A, XM_017028060.2:c.582G>A, XM_017028060.1:c.582G>A, NM_001319153.2:c.567G>A, NM_001319153.1:c.567G>A, NM_001319152.2:c.567G>A, NM_001319152.1:c.567G>A, XM_047440467.1:c.636G>A, XM_047440468.1:c.567G>A, XM_047440466.1:c.789G>A

Select item 14809891064.

rs1480989106 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 20:63556443 (GRCh38)
20:62187796 (GRCh37)
Canonical SPDI:: NC_000020.11:63556442:C:A
Gene:: FNDC11 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000028/1 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000020.11:g.63556443C>A, NC_000020.10:g.62187796C>A, XM_011529041.3:c.780C>A, XM_011529041.2:c.780C>A, XM_011529041.1:c.780C>A, NM_024059.3:c.780C>A, NM_024059.2:c.780C>A, XM_017028060.2:c.795C>A, XM_017028060.1:c.795C>A, NM_001319153.2:c.780C>A, NM_001319153.1:c.780C>A, NM_001319152.2:c.780C>A, NM_001319152.1:c.780C>A, XM_047440467.1:c.849C>A, XM_047440468.1:c.780C>A, XM_047440466.1:c.1002C>A

Select item 14770142995.

rs1477014299 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:63556677 (GRCh38)
20:62188030 (GRCh37)
Canonical SPDI:: NC_000020.11:63556676:A:G
Gene:: FNDC11 (Varview)
Functional Consequence:: 3_prime_UTR_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_000020.11:g.63556677A>G, NC_000020.10:g.62188030A>G, XM_011529041.3:c.*57A>G, XM_011529041.2:c.*57A>G, XM_011529041.1:c.*57A>G, NM_024059.3:c.*57A>G, NM_024059.2:c.*57A>G, XM_017028060.2:c.*57A>G, XM_017028060.1:c.*57A>G, NM_001319153.2:c.*57A>G, NM_001319153.1:c.*57A>G, NM_001319152.2:c.*57A>G, NM_001319152.1:c.*57A>G, XM_047440467.1:c.*57A>G, XM_047440468.1:c.*57A>G, XM_047440466.1:c.*57A>G

Select item 14757088966.

rs1475708896 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:63553091 (GRCh38)
20:62184444 (GRCh37)
Canonical SPDI:: NC_000020.11:63553090:T:C
Gene:: FNDC11 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.63553091T>C, NC_000020.10:g.62184444T>C, NM_024059.3:c.-21T>C, NM_024059.2:c.-21T>C, XM_047440468.1:c.-217T>C

Select item 14727857357.

rs1472785735 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63556474 (GRCh38)
20:62187827 (GRCh37)
Canonical SPDI:: NC_000020.11:63556473:C:T
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000028/7 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63556474C>T, NC_000020.10:g.62187827C>T, XM_011529041.3:c.811C>T, XM_011529041.2:c.811C>T, XM_011529041.1:c.811C>T, NM_024059.3:c.811C>T, NM_024059.2:c.811C>T, XM_017028060.2:c.826C>T, XM_017028060.1:c.826C>T, NM_001319153.2:c.811C>T, NM_001319153.1:c.811C>T, NM_001319152.2:c.811C>T, NM_001319152.1:c.811C>T, XM_047440467.1:c.880C>T, XM_047440468.1:c.811C>T, XM_047440466.1:c.1033C>T, XP_011527343.1:p.Arg271Ter, NP_076964.1:p.Arg271Ter, XP_016883549.1:p.Arg276Ter, NP_001306082.1:p.Arg271Ter, NP_001306081.1:p.Arg271Ter, XP_047296423.1:p.Arg294Ter, XP_047296424.1:p.Arg271Ter, XP_047296422.1:p.Arg345Ter

Select item 14717127488.

rs1471712748 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63556419 (GRCh38)
20:62187772 (GRCh37)
Canonical SPDI:: NC_000020.11:63556418:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: A=0.000008/2 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
A=0.001092/2 (Korea1K)
A=0.001369/4 (KOREAN)
HGVS:: NC_000020.11:g.63556419G>A, NC_000020.10:g.62187772G>A, XM_011529041.3:c.756G>A, XM_011529041.2:c.756G>A, XM_011529041.1:c.756G>A, NM_024059.3:c.756G>A, NM_024059.2:c.756G>A, XM_017028060.2:c.771G>A, XM_017028060.1:c.771G>A, NM_001319153.2:c.756G>A, NM_001319153.1:c.756G>A, NM_001319152.2:c.756G>A, NM_001319152.1:c.756G>A, XM_047440467.1:c.825G>A, XM_047440468.1:c.756G>A, XM_047440466.1:c.978G>A

Select item 14707020089.

rs1470702008 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63556346 (GRCh38)
20:62187699 (GRCh37)
Canonical SPDI:: NC_000020.11:63556345:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.63556346G>A, NC_000020.10:g.62187699G>A, XM_011529041.3:c.683G>A, XM_011529041.2:c.683G>A, XM_011529041.1:c.683G>A, NM_024059.3:c.683G>A, NM_024059.2:c.683G>A, XM_017028060.2:c.698G>A, XM_017028060.1:c.698G>A, NM_001319153.2:c.683G>A, NM_001319153.1:c.683G>A, NM_001319152.2:c.683G>A, NM_001319152.1:c.683G>A, XM_047440467.1:c.752G>A, XM_047440468.1:c.683G>A, XM_047440466.1:c.905G>A, XP_011527343.1:p.Trp228Ter, NP_076964.1:p.Trp228Ter, XP_016883549.1:p.Trp233Ter, NP_001306082.1:p.Trp228Ter, NP_001306081.1:p.Trp228Ter, XP_047296423.1:p.Trp251Ter, XP_047296424.1:p.Trp228Ter, XP_047296422.1:p.Trp302Ter

Select item 146838031310.

rs1468380313 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63555858 (GRCh38)
20:62187211 (GRCh37)
Canonical SPDI:: NC_000020.11:63555857:C:T
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.63555858C>T, NC_000020.10:g.62187211C>T, XM_011529041.3:c.195C>T, XM_011529041.2:c.195C>T, XM_011529041.1:c.195C>T, NM_024059.3:c.195C>T, NM_024059.2:c.195C>T, XM_017028060.2:c.210C>T, XM_017028060.1:c.210C>T, NM_001319153.2:c.195C>T, NM_001319153.1:c.195C>T, NM_001319152.2:c.195C>T, NM_001319152.1:c.195C>T, XM_047440467.1:c.264C>T, XM_047440468.1:c.195C>T, XM_047440466.1:c.417C>T

Select item 146573128811.

rs1465731288 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63555693 (GRCh38)
20:62187046 (GRCh37)
Canonical SPDI:: NC_000020.11:63555692:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000020.11:g.63555693G>A, NC_000020.10:g.62187046G>A, XM_011529041.3:c.30G>A, XM_011529041.2:c.30G>A, XM_011529041.1:c.30G>A, NM_024059.3:c.30G>A, NM_024059.2:c.30G>A, XM_017028060.2:c.45G>A, XM_017028060.1:c.45G>A, NM_001319153.2:c.30G>A, NM_001319153.1:c.30G>A, NM_001319152.2:c.30G>A, NM_001319152.1:c.30G>A, XM_047440467.1:c.99G>A, XM_047440468.1:c.30G>A, XM_047440466.1:c.252G>A

Select item 146569050512.

rs1465690505 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63556366 (GRCh38)
20:62187719 (GRCh37)
Canonical SPDI:: NC_000020.11:63556365:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000020.11:g.63556366G>A, NC_000020.10:g.62187719G>A, XM_011529041.3:c.703G>A, XM_011529041.2:c.703G>A, XM_011529041.1:c.703G>A, NM_024059.3:c.703G>A, NM_024059.2:c.703G>A, XM_017028060.2:c.718G>A, XM_017028060.1:c.718G>A, NM_001319153.2:c.703G>A, NM_001319153.1:c.703G>A, NM_001319152.2:c.703G>A, NM_001319152.1:c.703G>A, XM_047440467.1:c.772G>A, XM_047440468.1:c.703G>A, XM_047440466.1:c.925G>A, XP_011527343.1:p.Ala235Thr, NP_076964.1:p.Ala235Thr, XP_016883549.1:p.Ala240Thr, NP_001306082.1:p.Ala235Thr, NP_001306081.1:p.Ala235Thr, XP_047296423.1:p.Ala258Thr, XP_047296424.1:p.Ala235Thr, XP_047296422.1:p.Ala309Thr

Select item 146291373513.

rs1462913735 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63555736 (GRCh38)
20:62187089 (GRCh37)
Canonical SPDI:: NC_000020.11:63555735:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.63555736G>A, NC_000020.10:g.62187089G>A, XM_011529041.3:c.73G>A, XM_011529041.2:c.73G>A, XM_011529041.1:c.73G>A, NM_024059.3:c.73G>A, NM_024059.2:c.73G>A, XM_017028060.2:c.88G>A, XM_017028060.1:c.88G>A, NM_001319153.2:c.73G>A, NM_001319153.1:c.73G>A, NM_001319152.2:c.73G>A, NM_001319152.1:c.73G>A, XM_047440467.1:c.142G>A, XM_047440468.1:c.73G>A, XM_047440466.1:c.295G>A, XP_011527343.1:p.Glu25Lys, NP_076964.1:p.Glu25Lys, XP_016883549.1:p.Glu30Lys, NP_001306082.1:p.Glu25Lys, NP_001306081.1:p.Glu25Lys, XP_047296423.1:p.Glu48Lys, XP_047296424.1:p.Glu25Lys, XP_047296422.1:p.Glu99Lys

Select item 145986503414.

rs1459865034 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 20:63556252 (GRCh38)
20:62187605 (GRCh37)
Canonical SPDI:: NC_000020.11:63556251:A:T
Gene:: FNDC11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63556252A>T, NC_000020.10:g.62187605A>T, XM_011529041.3:c.589A>T, XM_011529041.2:c.589A>T, XM_011529041.1:c.589A>T, NM_024059.3:c.589A>T, NM_024059.2:c.589A>T, XM_017028060.2:c.604A>T, XM_017028060.1:c.604A>T, NM_001319153.2:c.589A>T, NM_001319153.1:c.589A>T, NM_001319152.2:c.589A>T, NM_001319152.1:c.589A>T, XM_047440467.1:c.658A>T, XM_047440468.1:c.589A>T, XM_047440466.1:c.811A>T, XP_011527343.1:p.Ile197Phe, NP_076964.1:p.Ile197Phe, XP_016883549.1:p.Ile202Phe, NP_001306082.1:p.Ile197Phe, NP_001306081.1:p.Ile197Phe, XP_047296423.1:p.Ile220Phe, XP_047296424.1:p.Ile197Phe, XP_047296422.1:p.Ile271Phe

Select item 145703014915.

rs1457030149 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63556145 (GRCh38)
20:62187498 (GRCh37)
Canonical SPDI:: NC_000020.11:63556144:G:A
Gene:: FNDC11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63556145G>A, NC_000020.10:g.62187498G>A, XM_011529041.3:c.482G>A, XM_011529041.2:c.482G>A, XM_011529041.1:c.482G>A, NM_024059.3:c.482G>A, NM_024059.2:c.482G>A, XM_017028060.2:c.497G>A, XM_017028060.1:c.497G>A, NM_001319153.2:c.482G>A, NM_001319153.1:c.482G>A, NM_001319152.2:c.482G>A, NM_001319152.1:c.482G>A, XM_047440467.1:c.551G>A, XM_047440468.1:c.482G>A, XM_047440466.1:c.704G>A, XP_011527343.1:p.Arg161Gln, NP_076964.1:p.Arg161Gln, XP_016883549.1:p.Arg166Gln, NP_001306082.1:p.Arg161Gln, NP_001306081.1:p.Arg161Gln, XP_047296423.1:p.Arg184Gln, XP_047296424.1:p.Arg161Gln, XP_047296422.1:p.Arg235Gln

Select item 145457838316.

rs1454578383 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 20:63556341 (GRCh38)
20:62187694 (GRCh37)
Canonical SPDI:: NC_000020.11:63556340:G:T
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63556341G>T, NC_000020.10:g.62187694G>T, XM_011529041.3:c.678G>T, XM_011529041.2:c.678G>T, XM_011529041.1:c.678G>T, NM_024059.3:c.678G>T, NM_024059.2:c.678G>T, XM_017028060.2:c.693G>T, XM_017028060.1:c.693G>T, NM_001319153.2:c.678G>T, NM_001319153.1:c.678G>T, NM_001319152.2:c.678G>T, NM_001319152.1:c.678G>T, XM_047440467.1:c.747G>T, XM_047440468.1:c.678G>T, XM_047440466.1:c.900G>T

Select item 145166973517.

rs1451669735 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:63556171 (GRCh38)
20:62187524 (GRCh37)
Canonical SPDI:: NC_000020.11:63556170:A:G
Gene:: FNDC11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000035/1 (TOMMO)
HGVS:: NC_000020.11:g.63556171A>G, NC_000020.10:g.62187524A>G, XM_011529041.3:c.508A>G, XM_011529041.2:c.508A>G, XM_011529041.1:c.508A>G, NM_024059.3:c.508A>G, NM_024059.2:c.508A>G, XM_017028060.2:c.523A>G, XM_017028060.1:c.523A>G, NM_001319153.2:c.508A>G, NM_001319153.1:c.508A>G, NM_001319152.2:c.508A>G, NM_001319152.1:c.508A>G, XM_047440467.1:c.577A>G, XM_047440468.1:c.508A>G, XM_047440466.1:c.730A>G, XP_011527343.1:p.Met170Val, NP_076964.1:p.Met170Val, XP_016883549.1:p.Met175Val, NP_001306082.1:p.Met170Val, NP_001306081.1:p.Met170Val, XP_047296423.1:p.Met193Val, XP_047296424.1:p.Met170Val, XP_047296422.1:p.Met244Val

Select item 145155827818.

rs1451558278 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 20:63555910 (GRCh38)
20:62187263 (GRCh37)
Canonical SPDI:: NC_000020.11:63555909:AA:A
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.63555911del, NC_000020.10:g.62187264del, XM_011529041.3:c.248del, XM_011529041.2:c.248del, XM_011529041.1:c.248del, NM_024059.3:c.248del, NM_024059.2:c.248del, XM_017028060.2:c.263del, XM_017028060.1:c.263del, NM_001319153.2:c.248del, NM_001319153.1:c.248del, NM_001319152.2:c.248del, NM_001319152.1:c.248del, XM_047440467.1:c.317del, XM_047440468.1:c.248del, XM_047440466.1:c.470del, XP_011527343.1:p.Lys83fs, NP_076964.1:p.Lys83fs, XP_016883549.1:p.Lys88fs, NP_001306082.1:p.Lys83fs, NP_001306081.1:p.Lys83fs, XP_047296423.1:p.Lys106fs, XP_047296424.1:p.Lys83fs, XP_047296422.1:p.Lys157fs

Select item 145015144519.

rs1450151445 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63556323 (GRCh38)
20:62187676 (GRCh37)
Canonical SPDI:: NC_000020.11:63556322:C:T
Gene:: FNDC11 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000020.11:g.63556323C>T, NC_000020.10:g.62187676C>T, XM_011529041.3:c.660C>T, XM_011529041.2:c.660C>T, XM_011529041.1:c.660C>T, NM_024059.3:c.660C>T, NM_024059.2:c.660C>T, XM_017028060.2:c.675C>T, XM_017028060.1:c.675C>T, NM_001319153.2:c.660C>T, NM_001319153.1:c.660C>T, NM_001319152.2:c.660C>T, NM_001319152.1:c.660C>T, XM_047440467.1:c.729C>T, XM_047440468.1:c.660C>T, XM_047440466.1:c.882C>T

Select item 144763590220.

rs1447635902 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63556072 (GRCh38)
20:62187425 (GRCh37)
Canonical SPDI:: NC_000020.11:63556071:C:T
Gene:: FNDC11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
HGVS:: NC_000020.11:g.63556072C>T, NC_000020.10:g.62187425C>T, XM_011529041.3:c.409C>T, XM_011529041.2:c.409C>T, XM_011529041.1:c.409C>T, NM_024059.3:c.409C>T, NM_024059.2:c.409C>T, XM_017028060.2:c.424C>T, XM_017028060.1:c.424C>T, NM_001319153.2:c.409C>T, NM_001319153.1:c.409C>T, NM_001319152.2:c.409C>T, NM_001319152.1:c.409C>T, XM_047440467.1:c.478C>T, XM_047440468.1:c.409C>T, XM_047440466.1:c.631C>T, XP_011527343.1:p.Arg137Cys, NP_076964.1:p.Arg137Cys, XP_016883549.1:p.Arg142Cys, NP_001306082.1:p.Arg137Cys, NP_001306081.1:p.Arg137Cys, XP_047296423.1:p.Arg160Cys, XP_047296424.1:p.Arg137Cys, XP_047296422.1:p.Arg211Cys

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