rs376332017

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Species

Homo sapiens

Symbol

rs376332017

Category

Variant

Variant type

SNP

Overlaps

WDR33

Location

2:127719807

Nucleotide Change

T>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)2:127719807T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000322313.9:c.2218A>G
• RefSeq:NM_018383.5:c.2218A>G

Show All 4

HGVS.p name

• ENSP00000325377:p.Met740Val
• NP_060853:p.Met740Val

Show All 4

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences