rs990206963

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Species

Homo sapiens

Symbol

rs990206963

Category

Variant

Variant type

SNP

Overlaps

AFG2A

Location

4:123057197

Nucleotide Change

T>C

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• (GRCh38)4:123057197T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000274008.5:c.2134-12T>C
• ENSEMBL:ENST00000422835.2:n.2176-12T>C

Show All 6

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences