rs931290479

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Species

Homo sapiens

Symbol

rs931290479

Category

Variant

Variant type

SNP

Overlaps

MAP3K15

Location

X:19488913

Nucleotide Change

T>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)X:19488913T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000338883.9:c.416A>G
• RefSeq:XM_047442100.1:c.416A>G

Show All 3

HGVS.p name

• ENSP00000345629:p.His139Arg
• XP_047298056:p.His139Arg

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences