rs1729196475

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Species

Homo sapiens

Symbol

rs1729196475

Category

Variant

Variant type

SNP

Overlaps

AFG2A

Location

4:122938119

Nucleotide Change

T>C

Most Severe Consequence

• splice region variant&intron variant

See all consequences

HGVS.g name

• (GRCh38)4:122938119T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000274008.5:c.1335-7T>C
• ENSEMBL:ENST00000422835.2:n.1377-7T>C

Show All 24

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences