rs1690443549

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Species

Homo sapiens

Symbol

rs1690443549

Category

Variant

Variant type

SNP

Overlaps

PLCL1

Location

2:197805200

Nucleotide Change

T>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)2:197805200T>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000428675.6:c.101T>A
• ENSEMBL:ENST00000435320.1:n.499T>A

Show All 3

HGVS.p name

• ENSP00000402861:p.Val34Glu
• NP_006217:p.Val34Glu

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences