rs371919822

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Species

Homo sapiens

Symbol

rs371919822

Category

Variant

Variant type

SNP

Overlaps

ENPP4

Location

6:46139651

Nucleotide Change

G>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000006.12:g.46139651G>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000321037.5:c.68G>C
• RefSeq:NM_014936.5:c.68G>C

HGVS.p name

• ENSP00000318066:p.Ser23Thr
• NP_055751:p.Ser23Thr

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences