rs369201413

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Species

Homo sapiens

Symbol

rs369201413

Category

Variant

Variant type

SNP

Overlaps

CTRB1

Location

16:75222788

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000016.10:g.75222788C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000361017.9:c.73C>A
• ENSEMBL:ENST00000495583.1:c.145C>A

HGVS.p name

• ENSP00000354294:p.His25Asn
• ENSP00000463301:p.His49Asn

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences