rs207460758

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Species

Homo sapiens

Symbol

rs207460758

Category

Variant

Variant type

SNP

Overlaps

TSEN15

Location

1:184107797

Nucleotide Change

T>C

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• (GRCh38)1:184107797T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000643916.1:n.306-5068T>C
• ENSEMBL:ENST00000644592.1:n.377-11923T>C

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences