rs207470406

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Species

Homo sapiens

Symbol

rs207470406

Category

Variant

Variant type

SNP

Overlaps

MSANTD3-TMEFF1

Location

9:100461971

Nucleotide Change

T>A

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_000009.12:g.100461971T>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000502978.1:c.79+19615T>A
• RefSeq:NM_001198812.1:c.418+19615T>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences