rs371043746

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Species

Homo sapiens

Symbol

rs371043746

Category

Variant

Variant type

SNP

Overlaps

SDE2

Location

1:225995349

Nucleotide Change

T>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)1:225995349T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000272091.8:c.155A>G
• RefSeq:NM_152608.4:c.155A>G

HGVS.p name

• ENSP00000272091:p.Asn52Ser
• NP_689821:p.Asn52Ser

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences