SNP Links for Protein (Select 58533165) - SNP

Links from Protein

Items: 1 to 20 of 239

<< First< Prev

Page of 12

Next >Last >>

Select item 14905881921.

rs1490588192 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 7:81743392 (GRCh38)
7:81372708 (GRCh37)
Canonical SPDI:: NC_000007.14:81743391:G:A,NC_000007.14:81743391:G:C,NC_000007.14:81743391:G:T
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
HGVS:: NC_000007.14:g.81743392G>A, NC_000007.14:g.81743392G>C, NC_000007.14:g.81743392G>T, NC_000007.13:g.81372708G>A, NC_000007.13:g.81372708G>C, NC_000007.13:g.81372708G>T, NG_016274.2:g.31745C>T, NG_016274.2:g.31745C>G, NG_016274.2:g.31745C>A, NM_000601.6:c.826C>T, NM_000601.6:c.826C>G, NM_000601.6:c.826C>A, NM_000601.5:c.826C>T, NM_000601.5:c.826C>G, NM_000601.5:c.826C>A, NM_000601.4:c.826C>T, NM_000601.4:c.826C>G, NM_000601.4:c.826C>A, NM_001010932.3:c.811C>T, NM_001010932.3:c.811C>G, NM_001010932.3:c.811C>A, NM_001010932.2:c.811C>T, NM_001010932.2:c.811C>G, NM_001010932.2:c.811C>A, NM_001010932.1:c.811C>T, NM_001010932.1:c.811C>G, NM_001010932.1:c.811C>A, NM_001010931.3:c.826C>T, NM_001010931.3:c.826C>G, NM_001010931.3:c.826C>A, NM_001010931.2:c.826C>T, NM_001010931.2:c.826C>G, NM_001010931.2:c.826C>A, NM_001010931.1:c.826C>T, NM_001010931.1:c.826C>G, NM_001010931.1:c.826C>A, NM_001010933.3:c.811C>T, NM_001010933.3:c.811C>G, NM_001010933.3:c.811C>A, NM_001010933.2:c.811C>T, NM_001010933.2:c.811C>G, NM_001010933.2:c.811C>A, NM_001010933.1:c.811C>T, NM_001010933.1:c.811C>G, NM_001010933.1:c.811C>A, XM_047420293.1:c.826C>T, XM_047420293.1:c.826C>G, XM_047420293.1:c.826C>A, NP_000592.3:p.Pro276Ser, NP_000592.3:p.Pro276Ala, NP_000592.3:p.Pro276Thr, NP_001010932.1:p.Pro271Ser, NP_001010932.1:p.Pro271Ala, NP_001010932.1:p.Pro271Thr, NP_001010931.1:p.Pro276Ser, NP_001010931.1:p.Pro276Ala, NP_001010931.1:p.Pro276Thr, NP_001010933.1:p.Pro271Ser, NP_001010933.1:p.Pro271Ala, NP_001010933.1:p.Pro271Thr, XP_047276249.1:p.Pro276Ser, XP_047276249.1:p.Pro276Ala, XP_047276249.1:p.Pro276Thr

Select item 14860905332.

rs1486090533 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:81745088 (GRCh38)
7:81374404 (GRCh37)
Canonical SPDI:: NC_000007.14:81745087:G:A,NC_000007.14:81745087:G:C
Gene:: HGF (Varview)
Functional Consequence:: stop_gained,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.81745088G>A, NC_000007.14:g.81745088G>C, NC_000007.13:g.81374404G>A, NC_000007.13:g.81374404G>C, NG_016274.2:g.30049C>T, NG_016274.2:g.30049C>G, NM_000601.6:c.658C>T, NM_000601.6:c.658C>G, NM_000601.5:c.658C>T, NM_000601.5:c.658C>G, NM_000601.4:c.658C>T, NM_000601.4:c.658C>G, NM_001010932.3:c.643C>T, NM_001010932.3:c.643C>G, NM_001010932.2:c.643C>T, NM_001010932.2:c.643C>G, NM_001010932.1:c.643C>T, NM_001010932.1:c.643C>G, NM_001010931.3:c.658C>T, NM_001010931.3:c.658C>G, NM_001010931.2:c.658C>T, NM_001010931.2:c.658C>G, NM_001010931.1:c.658C>T, NM_001010931.1:c.658C>G, NM_001010933.3:c.643C>T, NM_001010933.3:c.643C>G, NM_001010933.2:c.643C>T, NM_001010933.2:c.643C>G, NM_001010933.1:c.643C>T, NM_001010933.1:c.643C>G, XM_047420293.1:c.658C>T, XM_047420293.1:c.658C>G, NP_000592.3:p.Arg220Ter, NP_000592.3:p.Arg220Gly, NP_001010932.1:p.Arg215Ter, NP_001010932.1:p.Arg215Gly, NP_001010931.1:p.Arg220Ter, NP_001010931.1:p.Arg220Gly, NP_001010933.1:p.Arg215Ter, NP_001010933.1:p.Arg215Gly, XP_047276249.1:p.Arg220Ter, XP_047276249.1:p.Arg220Gly

Select item 14851519583.

rs1485151958 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:81769904 (GRCh38)
7:81399220 (GRCh37)
Canonical SPDI:: NC_000007.14:81769903:G:A
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000007.14:g.81769904G>A, NC_000007.13:g.81399220G>A, NG_016274.2:g.5233C>T, NM_000601.6:c.68C>T, NM_000601.5:c.68C>T, NM_000601.4:c.68C>T, NM_001010932.3:c.68C>T, NM_001010932.2:c.68C>T, NM_001010932.1:c.68C>T, NM_001010934.3:c.68C>T, NM_001010934.2:c.68C>T, NM_001010934.1:c.68C>T, NM_001010931.3:c.68C>T, NM_001010931.2:c.68C>T, NM_001010931.1:c.68C>T, NM_001010933.3:c.68C>T, NM_001010933.2:c.68C>T, NM_001010933.1:c.68C>T, XM_047420293.1:c.68C>T, NP_000592.3:p.Pro23Leu, NP_001010932.1:p.Pro23Leu, NP_001010934.1:p.Pro23Leu, NP_001010931.1:p.Pro23Leu, NP_001010933.1:p.Pro23Leu, XP_047276249.1:p.Pro23Leu

Select item 14787623204.

rs1478762320 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:81762768 (GRCh38)
7:81392084 (GRCh37)
Canonical SPDI:: NC_000007.14:81762767:T:A
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_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=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.81762768T>A, NC_000007.13:g.81392084T>A, NG_016274.2:g.12369A>T, NM_000601.6:c.193A>T, NM_000601.5:c.193A>T, NM_000601.4:c.193A>T, NM_001010932.3:c.193A>T, NM_001010932.2:c.193A>T, NM_001010932.1:c.193A>T, NM_001010934.3:c.193A>T, NM_001010934.2:c.193A>T, NM_001010934.1:c.193A>T, NM_001010931.3:c.193A>T, NM_001010931.2:c.193A>T, NM_001010931.1:c.193A>T, NM_001010933.3:c.193A>T, NM_001010933.2:c.193A>T, NM_001010933.1:c.193A>T, XM_047420293.1:c.193A>T, NP_000592.3:p.Asn65Tyr, NP_001010932.1:p.Asn65Tyr, NP_001010934.1:p.Asn65Tyr, NP_001010931.1:p.Asn65Tyr, NP_001010933.1:p.Asn65Tyr, XP_047276249.1:p.Asn65Tyr

Select item 14763851695.

rs1476385169 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 7:81745045 (GRCh38)
7:81374361 (GRCh37)
Canonical SPDI:: NC_000007.14:81745044:C:A,NC_000007.14:81745044:C:G,NC_000007.14:81745044:C:T
Gene:: HGF (Varview)
Functional Consequence:: genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000007.14:g.81745045C>A, NC_000007.14:g.81745045C>G, NC_000007.14:g.81745045C>T, NC_000007.13:g.81374361C>A, NC_000007.13:g.81374361C>G, NC_000007.13:g.81374361C>T, NG_016274.2:g.30092G>T, NG_016274.2:g.30092G>C, NG_016274.2:g.30092G>A, NM_000601.6:c.701G>T, NM_000601.6:c.701G>C, NM_000601.6:c.701G>A, NM_000601.5:c.701G>T, NM_000601.5:c.701G>C, NM_000601.5:c.701G>A, NM_000601.4:c.701G>T, NM_000601.4:c.701G>C, NM_000601.4:c.701G>A, NM_001010932.3:c.686G>T, NM_001010932.3:c.686G>C, NM_001010932.3:c.686G>A, NM_001010932.2:c.686G>T, NM_001010932.2:c.686G>C, NM_001010932.2:c.686G>A, NM_001010932.1:c.686G>T, NM_001010932.1:c.686G>C, NM_001010932.1:c.686G>A, NM_001010931.3:c.701G>T, NM_001010931.3:c.701G>C, NM_001010931.3:c.701G>A, NM_001010931.2:c.701G>T, NM_001010931.2:c.701G>C, NM_001010931.2:c.701G>A, NM_001010931.1:c.701G>T, NM_001010931.1:c.701G>C, NM_001010931.1:c.701G>A, NM_001010933.3:c.686G>T, NM_001010933.3:c.686G>C, NM_001010933.3:c.686G>A, NM_001010933.2:c.686G>T, NM_001010933.2:c.686G>C, NM_001010933.2:c.686G>A, NM_001010933.1:c.686G>T, NM_001010933.1:c.686G>C, NM_001010933.1:c.686G>A, XM_047420293.1:c.701G>T, XM_047420293.1:c.701G>C, XM_047420293.1:c.701G>A, NP_000592.3:p.Arg234Leu, NP_000592.3:p.Arg234Pro, NP_000592.3:p.Arg234His, NP_001010932.1:p.Arg229Leu, NP_001010932.1:p.Arg229Pro, NP_001010932.1:p.Arg229His, NP_001010931.1:p.Arg234Leu, NP_001010931.1:p.Arg234Pro, NP_001010931.1:p.Arg234His, NP_001010933.1:p.Arg229Leu, NP_001010933.1:p.Arg229Pro, NP_001010933.1:p.Arg229His, XP_047276249.1:p.Arg234Leu, XP_047276249.1:p.Arg234Pro, XP_047276249.1:p.Arg234His

Select item 14757275606.

rs1475727560 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:81758739 (GRCh38)
7:81388055 (GRCh37)
Canonical SPDI:: NC_000007.14:81758738:C:G,NC_000007.14:81758738:C:T
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.81758739C>G, NC_000007.14:g.81758739C>T, NC_000007.13:g.81388055C>G, NC_000007.13:g.81388055C>T, NG_016274.2:g.16398G>C, NG_016274.2:g.16398G>A, NM_000601.6:c.320G>C, NM_000601.6:c.320G>A, NM_000601.5:c.320G>C, NM_000601.5:c.320G>A, NM_000601.4:c.320G>C, NM_000601.4:c.320G>A, NM_001010932.3:c.320G>C, NM_001010932.3:c.320G>A, NM_001010932.2:c.320G>C, NM_001010932.2:c.320G>A, NM_001010932.1:c.320G>C, NM_001010932.1:c.320G>A, NM_001010934.3:c.320G>C, NM_001010934.3:c.320G>A, NM_001010934.2:c.320G>C, NM_001010934.2:c.320G>A, NM_001010934.1:c.320G>C, NM_001010934.1:c.320G>A, NM_001010931.3:c.320G>C, NM_001010931.3:c.320G>A, NM_001010931.2:c.320G>C, NM_001010931.2:c.320G>A, NM_001010931.1:c.320G>C, NM_001010931.1:c.320G>A, NM_001010933.3:c.320G>C, NM_001010933.3:c.320G>A, NM_001010933.2:c.320G>C, NM_001010933.2:c.320G>A, NM_001010933.1:c.320G>C, NM_001010933.1:c.320G>A, XM_047420293.1:c.320G>C, XM_047420293.1:c.320G>A, NP_000592.3:p.Gly107Ala, NP_000592.3:p.Gly107Glu, NP_001010932.1:p.Gly107Ala, NP_001010932.1:p.Gly107Glu, NP_001010934.1:p.Gly107Ala, NP_001010934.1:p.Gly107Glu, NP_001010931.1:p.Gly107Ala, NP_001010931.1:p.Gly107Glu, NP_001010933.1:p.Gly107Ala, NP_001010933.1:p.Gly107Glu, XP_047276249.1:p.Gly107Ala, XP_047276249.1:p.Gly107Glu

Select item 14755506897.

rs1475550689 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 7:81762854 (GRCh38)
7:81392170 (GRCh37)
Canonical SPDI:: NC_000007.14:81762853:C:A,NC_000007.14:81762853:C:T
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by cluster
HGVS:: NC_000007.14:g.81762854C>A, NC_000007.14:g.81762854C>T, NC_000007.13:g.81392170C>A, NC_000007.13:g.81392170C>T, NG_016274.2:g.12283G>T, NG_016274.2:g.12283G>A, NM_000601.6:c.107G>T, NM_000601.6:c.107G>A, NM_000601.5:c.107G>T, NM_000601.5:c.107G>A, NM_000601.4:c.107G>T, NM_000601.4:c.107G>A, NM_001010932.3:c.107G>T, NM_001010932.3:c.107G>A, NM_001010932.2:c.107G>T, NM_001010932.2:c.107G>A, NM_001010932.1:c.107G>T, NM_001010932.1:c.107G>A, NM_001010934.3:c.107G>T, NM_001010934.3:c.107G>A, NM_001010934.2:c.107G>T, NM_001010934.2:c.107G>A, NM_001010934.1:c.107G>T, NM_001010934.1:c.107G>A, NM_001010931.3:c.107G>T, NM_001010931.3:c.107G>A, NM_001010931.2:c.107G>T, NM_001010931.2:c.107G>A, NM_001010931.1:c.107G>T, NM_001010931.1:c.107G>A, NM_001010933.3:c.107G>T, NM_001010933.3:c.107G>A, NM_001010933.2:c.107G>T, NM_001010933.2:c.107G>A, NM_001010933.1:c.107G>T, NM_001010933.1:c.107G>A, XM_047420293.1:c.107G>T, XM_047420293.1:c.107G>A, NP_000592.3:p.Arg36Ile, NP_000592.3:p.Arg36Lys, NP_001010932.1:p.Arg36Ile, NP_001010932.1:p.Arg36Lys, NP_001010934.1:p.Arg36Ile, NP_001010934.1:p.Arg36Lys, NP_001010931.1:p.Arg36Ile, NP_001010931.1:p.Arg36Lys, NP_001010933.1:p.Arg36Ile, NP_001010933.1:p.Arg36Lys, XP_047276249.1:p.Arg36Ile, XP_047276249.1:p.Arg36Lys

Select item 14675411828.

rs1467541182 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:81762749 (GRCh38)
7:81392065 (GRCh37)
Canonical SPDI:: NC_000007.14:81762748:G:A
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.81762749G>A, NC_000007.13:g.81392065G>A, NG_016274.2:g.12388C>T, NM_000601.6:c.212C>T, NM_000601.5:c.212C>T, NM_000601.4:c.212C>T, NM_001010932.3:c.212C>T, NM_001010932.2:c.212C>T, NM_001010932.1:c.212C>T, NM_001010934.3:c.212C>T, NM_001010934.2:c.212C>T, NM_001010934.1:c.212C>T, NM_001010931.3:c.212C>T, NM_001010931.2:c.212C>T, NM_001010931.1:c.212C>T, NM_001010933.3:c.212C>T, NM_001010933.2:c.212C>T, NM_001010933.1:c.212C>T, XM_047420293.1:c.212C>T, NP_000592.3:p.Ala71Val, NP_001010932.1:p.Ala71Val, NP_001010934.1:p.Ala71Val, NP_001010931.1:p.Ala71Val, NP_001010933.1:p.Ala71Val, XP_047276249.1:p.Ala71Val

Select item 14637386319.

rs1463738631 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:81743432 (GRCh38)
7:81372748 (GRCh37)
Canonical SPDI:: NC_000007.14:81743431:A:G
Gene:: HGF (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.81743432A>G, NC_000007.13:g.81372748A>G, NG_016274.2:g.31705T>C, NM_000601.6:c.786T>C, NM_000601.5:c.786T>C, NM_000601.4:c.786T>C, NM_001010932.3:c.771T>C, NM_001010932.2:c.771T>C, NM_001010932.1:c.771T>C, NM_001010931.3:c.786T>C, NM_001010931.2:c.786T>C, NM_001010931.1:c.786T>C, NM_001010933.3:c.771T>C, NM_001010933.2:c.771T>C, NM_001010933.1:c.771T>C, XM_047420293.1:c.786T>C

Select item 145281392110.

rs1452813921 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 7:81762836 (GRCh38)
7:81392152 (GRCh37)
Canonical SPDI:: NC_000007.14:81762835:A:T
Gene:: HGF (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000007.14:g.81762836A>T, NC_000007.13:g.81392152A>T, NG_016274.2:g.12301T>A, NM_000601.6:c.125T>A, NM_000601.5:c.125T>A, NM_000601.4:c.125T>A, NM_001010932.3:c.125T>A, NM_001010932.2:c.125T>A, NM_001010932.1:c.125T>A, NM_001010934.3:c.125T>A, NM_001010934.2:c.125T>A, NM_001010934.1:c.125T>A, NM_001010931.3:c.125T>A, NM_001010931.2:c.125T>A, NM_001010931.1:c.125T>A, NM_001010933.3:c.125T>A, NM_001010933.2:c.125T>A, NM_001010933.1:c.125T>A, XM_047420293.1:c.125T>A, NP_000592.3:p.Phe42Tyr, NP_001010932.1:p.Phe42Tyr, NP_001010934.1:p.Phe42Tyr, NP_001010931.1:p.Phe42Tyr, NP_001010933.1:p.Phe42Tyr, XP_047276249.1:p.Phe42Tyr

Select item 145028999811.

rs1450289998 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:81762844 (GRCh38)
7:81392160 (GRCh37)
Canonical SPDI:: NC_000007.14:81762843:A:G
Gene:: HGF (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0.000084/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.81762844A>G, NC_000007.13:g.81392160A>G, NG_016274.2:g.12293T>C, NM_000601.6:c.117T>C, NM_000601.5:c.117T>C, NM_000601.4:c.117T>C, NM_001010932.3:c.117T>C, NM_001010932.2:c.117T>C, NM_001010932.1:c.117T>C, NM_001010934.3:c.117T>C, NM_001010934.2:c.117T>C, NM_001010934.1:c.117T>C, NM_001010931.3:c.117T>C, NM_001010931.2:c.117T>C, NM_001010931.1:c.117T>C, NM_001010933.3:c.117T>C, NM_001010933.2:c.117T>C, NM_001010933.1:c.117T>C, XM_047420293.1:c.117T>C

Select item 144770806412.

rs1447708064 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 7:81743426 (GRCh38)
7:81372742 (GRCh37)
Canonical SPDI:: NC_000007.14:81743425:A:C,NC_000007.14:81743425:A:G,NC_000007.14:81743425:A:T
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.81743426A>C, NC_000007.14:g.81743426A>G, NC_000007.14:g.81743426A>T, NC_000007.13:g.81372742A>C, NC_000007.13:g.81372742A>G, NC_000007.13:g.81372742A>T, NG_016274.2:g.31711T>G, NG_016274.2:g.31711T>C, NG_016274.2:g.31711T>A, NM_000601.6:c.792T>G, NM_000601.6:c.792T>C, NM_000601.6:c.792T>A, NM_000601.5:c.792T>G, NM_000601.5:c.792T>C, NM_000601.5:c.792T>A, NM_000601.4:c.792T>G, NM_000601.4:c.792T>C, NM_000601.4:c.792T>A, NM_001010932.3:c.777T>G, NM_001010932.3:c.777T>C, NM_001010932.3:c.777T>A, NM_001010932.2:c.777T>G, NM_001010932.2:c.777T>C, NM_001010932.2:c.777T>A, NM_001010932.1:c.777T>G, NM_001010932.1:c.777T>C, NM_001010932.1:c.777T>A, NM_001010931.3:c.792T>G, NM_001010931.3:c.792T>C, NM_001010931.3:c.792T>A, NM_001010931.2:c.792T>G, NM_001010931.2:c.792T>C, NM_001010931.2:c.792T>A, NM_001010931.1:c.792T>G, NM_001010931.1:c.792T>C, NM_001010931.1:c.792T>A, NM_001010933.3:c.777T>G, NM_001010933.3:c.777T>C, NM_001010933.3:c.777T>A, NM_001010933.2:c.777T>G, NM_001010933.2:c.777T>C, NM_001010933.2:c.777T>A, NM_001010933.1:c.777T>G, NM_001010933.1:c.777T>C, NM_001010933.1:c.777T>A, XM_047420293.1:c.792T>G, XM_047420293.1:c.792T>C, XM_047420293.1:c.792T>A, NP_000592.3:p.Asp264Glu, NP_000592.3:p.Asp264Glu, NP_001010932.1:p.Asp259Glu, NP_001010932.1:p.Asp259Glu, NP_001010931.1:p.Asp264Glu, NP_001010931.1:p.Asp264Glu, NP_001010933.1:p.Asp259Glu, NP_001010933.1:p.Asp259Glu, XP_047276249.1:p.Asp264Glu, XP_047276249.1:p.Asp264Glu

Select item 144371158513.

rs1443711585 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:81762798 (GRCh38)
7:81392114 (GRCh37)
Canonical SPDI:: NC_000007.14:81762797:G:C
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000007.14:g.81762798G>C, NC_000007.13:g.81392114G>C, NG_016274.2:g.12339C>G, NM_000601.6:c.163C>G, NM_000601.5:c.163C>G, NM_000601.4:c.163C>G, NM_001010932.3:c.163C>G, NM_001010932.2:c.163C>G, NM_001010932.1:c.163C>G, NM_001010934.3:c.163C>G, NM_001010934.2:c.163C>G, NM_001010934.1:c.163C>G, NM_001010931.3:c.163C>G, NM_001010931.2:c.163C>G, NM_001010931.1:c.163C>G, NM_001010933.3:c.163C>G, NM_001010933.2:c.163C>G, NM_001010933.1:c.163C>G, XM_047420293.1:c.163C>G, NP_000592.3:p.Pro55Ala, NP_001010932.1:p.Pro55Ala, NP_001010934.1:p.Pro55Ala, NP_001010931.1:p.Pro55Ala, NP_001010933.1:p.Pro55Ala, XP_047276249.1:p.Pro55Ala

Select item 143998134814.

rs1439981348 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 7:81752138 (GRCh38)
7:81381454 (GRCh37)
Canonical SPDI:: NC_000007.14:81752137:T:A,NC_000007.14:81752137:T:G
Gene:: HGF (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.81752138T>A, NC_000007.14:g.81752138T>G, NC_000007.13:g.81381454T>A, NC_000007.13:g.81381454T>G, NG_016274.2:g.22999A>T, NG_016274.2:g.22999A>C, NM_000601.6:c.607A>T, NM_000601.6:c.607A>C, NM_000601.5:c.607A>T, NM_000601.5:c.607A>C, NM_000601.4:c.607A>T, NM_000601.4:c.607A>C, NM_001010932.3:c.592A>T, NM_001010932.3:c.592A>C, NM_001010932.2:c.592A>T, NM_001010932.2:c.592A>C, NM_001010932.1:c.592A>T, NM_001010932.1:c.592A>C, NM_001010934.3:c.607A>T, NM_001010934.3:c.607A>C, NM_001010934.2:c.607A>T, NM_001010934.2:c.607A>C, NM_001010934.1:c.607A>T, NM_001010934.1:c.607A>C, NM_001010931.3:c.607A>T, NM_001010931.3:c.607A>C, NM_001010931.2:c.607A>T, NM_001010931.2:c.607A>C, NM_001010931.1:c.607A>T, NM_001010931.1:c.607A>C, NM_001010933.3:c.592A>T, NM_001010933.3:c.592A>C, NM_001010933.2:c.592A>T, NM_001010933.2:c.592A>C, NM_001010933.1:c.592A>T, NM_001010933.1:c.592A>C, XM_047420293.1:c.607A>T, XM_047420293.1:c.607A>C, NP_000592.3:p.Ile203Phe, NP_000592.3:p.Ile203Leu, NP_001010932.1:p.Ile198Phe, NP_001010932.1:p.Ile198Leu, NP_001010934.1:p.Ile203Phe, NP_001010934.1:p.Ile203Leu, NP_001010931.1:p.Ile203Phe, NP_001010931.1:p.Ile203Leu, NP_001010933.1:p.Ile198Phe, NP_001010933.1:p.Ile198Leu, XP_047276249.1:p.Ile203Phe, XP_047276249.1:p.Ile203Leu

Select item 143435447315.

rs1434354473 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:81769930 (GRCh38)
7:81399246 (GRCh37)
Canonical SPDI:: NC_000007.14:81769929:A:G
Gene:: HGF (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.81769930A>G, NC_000007.13:g.81399246A>G, NG_016274.2:g.5207T>C, NM_000601.6:c.42T>C, NM_000601.5:c.42T>C, NM_000601.4:c.42T>C, NM_001010932.3:c.42T>C, NM_001010932.2:c.42T>C, NM_001010932.1:c.42T>C, NM_001010934.3:c.42T>C, NM_001010934.2:c.42T>C, NM_001010934.1:c.42T>C, NM_001010931.3:c.42T>C, NM_001010931.2:c.42T>C, NM_001010931.1:c.42T>C, NM_001010933.3:c.42T>C, NM_001010933.2:c.42T>C, NM_001010933.1:c.42T>C, XM_047420293.1:c.42T>C

Select item 143282599516.

rs1432825995 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 7:81752225 (GRCh38)
7:81381541 (GRCh37)
Canonical SPDI:: NC_000007.14:81752224:C:A,NC_000007.14:81752224:C:G,NC_000007.14:81752224:C:T
Gene:: HGF (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000007.14:g.81752225C>A, NC_000007.14:g.81752225C>G, NC_000007.14:g.81752225C>T, NC_000007.13:g.81381541C>A, NC_000007.13:g.81381541C>G, NC_000007.13:g.81381541C>T, NG_016274.2:g.22912G>T, NG_016274.2:g.22912G>C, NG_016274.2:g.22912G>A, NM_000601.6:c.520G>T, NM_000601.6:c.520G>C, NM_000601.6:c.520G>A, NM_000601.5:c.520G>T, NM_000601.5:c.520G>C, NM_000601.5:c.520G>A, NM_000601.4:c.520G>T, NM_000601.4:c.520G>C, NM_000601.4:c.520G>A, NM_001010932.3:c.505G>T, NM_001010932.3:c.505G>C, NM_001010932.3:c.505G>A, NM_001010932.2:c.505G>T, NM_001010932.2:c.505G>C, NM_001010932.2:c.505G>A, NM_001010932.1:c.505G>T, NM_001010932.1:c.505G>C, NM_001010932.1:c.505G>A, NM_001010934.3:c.520G>T, NM_001010934.3:c.520G>C, NM_001010934.3:c.520G>A, NM_001010934.2:c.520G>T, NM_001010934.2:c.520G>C, NM_001010934.2:c.520G>A, NM_001010934.1:c.520G>T, NM_001010934.1:c.520G>C, NM_001010934.1:c.520G>A, NM_001010931.3:c.520G>T, NM_001010931.3:c.520G>C, NM_001010931.3:c.520G>A, NM_001010931.2:c.520G>T, NM_001010931.2:c.520G>C, NM_001010931.2:c.520G>A, NM_001010931.1:c.520G>T, NM_001010931.1:c.520G>C, NM_001010931.1:c.520G>A, NM_001010933.3:c.505G>T, NM_001010933.3:c.505G>C, NM_001010933.3:c.505G>A, NM_001010933.2:c.505G>T, NM_001010933.2:c.505G>C, NM_001010933.2:c.505G>A, NM_001010933.1:c.505G>T, NM_001010933.1:c.505G>C, NM_001010933.1:c.505G>A, XM_047420293.1:c.520G>T, XM_047420293.1:c.520G>C, XM_047420293.1:c.520G>A, NP_000592.3:p.Glu174Ter, NP_000592.3:p.Glu174Gln, NP_000592.3:p.Glu174Lys, NP_001010932.1:p.Glu169Ter, NP_001010932.1:p.Glu169Gln, NP_001010932.1:p.Glu169Lys, NP_001010934.1:p.Glu174Ter, NP_001010934.1:p.Glu174Gln, NP_001010934.1:p.Glu174Lys, NP_001010931.1:p.Glu174Ter, NP_001010931.1:p.Glu174Gln, NP_001010931.1:p.Glu174Lys, NP_001010933.1:p.Glu169Ter, NP_001010933.1:p.Glu169Gln, NP_001010933.1:p.Glu169Lys, XP_047276249.1:p.Glu174Ter, XP_047276249.1:p.Glu174Gln, XP_047276249.1:p.Glu174Lys

Select item 142737539317.

rs1427375393 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:81757254 (GRCh38)
7:81386570 (GRCh37)
Canonical SPDI:: NC_000007.14:81757253:T:C
Gene:: HGF (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.81757254T>C, NC_000007.13:g.81386570T>C, NG_016274.2:g.17883A>G, NM_000601.6:c.417A>G, NM_000601.5:c.417A>G, NM_000601.4:c.417A>G, NM_001010932.3:c.417A>G, NM_001010932.2:c.417A>G, NM_001010932.1:c.417A>G, NM_001010934.3:c.417A>G, NM_001010934.2:c.417A>G, NM_001010934.1:c.417A>G, NM_001010931.3:c.417A>G, NM_001010931.2:c.417A>G, NM_001010931.1:c.417A>G, NM_001010933.3:c.417A>G, NM_001010933.2:c.417A>G, NM_001010933.1:c.417A>G, XM_047420293.1:c.417A>G

Select item 142546792118.

rs1425467921 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 7:81757232 (GRCh38)
7:81386548 (GRCh37)
Canonical SPDI:: NC_000007.14:81757231:T:A,NC_000007.14:81757231:T:C
Gene:: HGF (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_000007.14:g.81757232T>A, NC_000007.14:g.81757232T>C, NC_000007.13:g.81386548T>A, NC_000007.13:g.81386548T>C, NG_016274.2:g.17905A>T, NG_016274.2:g.17905A>G, NM_000601.6:c.439A>T, NM_000601.6:c.439A>G, NM_000601.5:c.439A>T, NM_000601.5:c.439A>G, NM_000601.4:c.439A>T, NM_000601.4:c.439A>G, NM_001010932.3:c.439A>T, NM_001010932.3:c.439A>G, NM_001010932.2:c.439A>T, NM_001010932.2:c.439A>G, NM_001010932.1:c.439A>T, NM_001010932.1:c.439A>G, NM_001010934.3:c.439A>T, NM_001010934.3:c.439A>G, NM_001010934.2:c.439A>T, NM_001010934.2:c.439A>G, NM_001010934.1:c.439A>T, NM_001010934.1:c.439A>G, NM_001010931.3:c.439A>T, NM_001010931.3:c.439A>G, NM_001010931.2:c.439A>T, NM_001010931.2:c.439A>G, NM_001010931.1:c.439A>T, NM_001010931.1:c.439A>G, NM_001010933.3:c.439A>T, NM_001010933.3:c.439A>G, NM_001010933.2:c.439A>T, NM_001010933.2:c.439A>G, NM_001010933.1:c.439A>T, NM_001010933.1:c.439A>G, XM_047420293.1:c.439A>T, XM_047420293.1:c.439A>G, NP_000592.3:p.Ile147Phe, NP_000592.3:p.Ile147Val, NP_001010932.1:p.Ile147Phe, NP_001010932.1:p.Ile147Val, NP_001010934.1:p.Ile147Phe, NP_001010934.1:p.Ile147Val, NP_001010931.1:p.Ile147Phe, NP_001010931.1:p.Ile147Val, NP_001010933.1:p.Ile147Phe, NP_001010933.1:p.Ile147Val, XP_047276249.1:p.Ile147Phe, XP_047276249.1:p.Ile147Val

Select item 141841350019.

rs1418413500 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 7:81762775 (GRCh38)
7:81392091 (GRCh37)
Canonical SPDI:: NC_000007.14:81762774:T:C,NC_000007.14:81762774:T:G
Gene:: HGF (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000007.14:g.81762775T>C, NC_000007.14:g.81762775T>G, NC_000007.13:g.81392091T>C, NC_000007.13:g.81392091T>G, NG_016274.2:g.12362A>G, NG_016274.2:g.12362A>C, NM_000601.6:c.186A>G, NM_000601.6:c.186A>C, NM_000601.5:c.186A>G, NM_000601.5:c.186A>C, NM_000601.4:c.186A>G, NM_000601.4:c.186A>C, NM_001010932.3:c.186A>G, NM_001010932.3:c.186A>C, NM_001010932.2:c.186A>G, NM_001010932.2:c.186A>C, NM_001010932.1:c.186A>G, NM_001010932.1:c.186A>C, NM_001010934.3:c.186A>G, NM_001010934.3:c.186A>C, NM_001010934.2:c.186A>G, NM_001010934.2:c.186A>C, NM_001010934.1:c.186A>G, NM_001010934.1:c.186A>C, NM_001010931.3:c.186A>G, NM_001010931.3:c.186A>C, NM_001010931.2:c.186A>G, NM_001010931.2:c.186A>C, NM_001010931.1:c.186A>G, NM_001010931.1:c.186A>C, NM_001010933.3:c.186A>G, NM_001010933.3:c.186A>C, NM_001010933.2:c.186A>G, NM_001010933.2:c.186A>C, NM_001010933.1:c.186A>G, NM_001010933.1:c.186A>C, XM_047420293.1:c.186A>G, XM_047420293.1:c.186A>C, NP_000592.3:p.Lys62Asn, NP_001010932.1:p.Lys62Asn, NP_001010934.1:p.Lys62Asn, NP_001010931.1:p.Lys62Asn, NP_001010933.1:p.Lys62Asn, XP_047276249.1:p.Lys62Asn

Select item 141318835020.

rs1413188350 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:81762868 (GRCh38)
7:81392184 (GRCh37)
Canonical SPDI:: NC_000007.14:81762867:T:A
Gene:: HGF (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.81762868T>A, NC_000007.13:g.81392184T>A, NG_016274.2:g.12269A>T, NM_000601.6:c.93A>T, NM_000601.5:c.93A>T, NM_000601.4:c.93A>T, NM_001010932.3:c.93A>T, NM_001010932.2:c.93A>T, NM_001010932.1:c.93A>T, NM_001010934.3:c.93A>T, NM_001010934.2:c.93A>T, NM_001010934.1:c.93A>T, NM_001010931.3:c.93A>T, NM_001010931.2:c.93A>T, NM_001010931.1:c.93A>T, NM_001010933.3:c.93A>T, NM_001010933.2:c.93A>T, NM_001010933.1:c.93A>T, XM_047420293.1:c.93A>T

<< First< Prev

Page of 12

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 239

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity