rs369277829

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Species

Homo sapiens

Symbol

rs369277829

Category

Variant

Variant type

SNP

Overlaps

DUSP12

Location

1:161753143

Nucleotide Change

A>C

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• (GRCh38)1:161753143A>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000367943.5:c.743A>C
• ENSEMBL:ENST00000463365.1:n.135A>C

Show All 4

HGVS.p name

• ENSP00000356920:p.His248Pro

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences