rs201716905

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Species

Homo sapiens

Symbol

rs201716905

Category

Variant

Variant type

SNP

Overlaps

RBKS

Location

2:27843079

Nucleotide Change

G>A

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• (GRCh38)2:27843079G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000302188.8:c.502C>T
• ENSEMBL:ENST00000448427.1:n.204-51454G>A

Show All 4

HGVS.p name

• ENSP00000306817:p.Arg168Cys
• ENSP00000393558:p.Pro28Leu

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences