rs1221106213

---

Species

Homo sapiens

Symbol

rs1221106213

Category

Variant

Variant type

SNP

Overlaps

SCD5

Location

4:82636662

Nucleotide Change

A>G

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)4:82636662A>G

Show All 5

HGVS.c name

• ENSEMBL:ENST00000319540.9:c.731T>C
• RefSeq:NM_001037582.3:c.731T>C

HGVS.p name

• ENSP00000316329:p.Met244Thr
• NP_001032671:p.Met244Thr

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences