rs754707908

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Species

Homo sapiens

Symbol

rs754707908

Category

Variant

Variant type

SNP

Overlaps

MAP3K15

Location

X:19515011

Nucleotide Change

C>G

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)X:19515011C>G

Show All 5

HGVS.c name

• ENSEMBL:ENST00000338883.9:c.251G>C
• RefSeq:XM_047442100.1:c.251G>C

Show All 3

HGVS.p name

• ENSP00000345629:p.Arg84Pro
• XP_047298056:p.Arg84Pro

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences