rs207462783

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Species

Homo sapiens

Symbol

rs207462783

Category

Variant

Variant type

SNP

Overlaps

PLCL1

Location

2:198248982

Nucleotide Change

C>A

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• (GRCh38)2:198248982C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000625084.1:n.44+99564C>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences