rs2106112941

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Species

Homo sapiens

Symbol

rs2106112941

Category

Variant

Variant type

SNP

Overlaps

OBSL1

Location

2:219570255

Nucleotide Change

G>C

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• NC_000002.12:g.219570255G>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000289656.3:c.-228+1139C>G
• ENSEMBL:ENST00000373873.8:c.978C>G

Show All 11

HGVS.p name

• ENSP00000362980:p.Gly326=
• ENSP00000362983:p.Gly326=

Show All 7

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences