rs780916397

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Species

Homo sapiens

Symbol

rs780916397

Category

Variant

Variant type

SNP

Overlaps

SOWAHD

Location

X:119759217

Nucleotide Change

G>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)X:119759217G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000343905.5:c.550G>A
• RefSeq:NM_001105576.3:c.550G>A

HGVS.p name

• ENSP00000340975:p.Gly184Ser
• NP_001099046:p.Gly184Ser

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences