rs1553868765

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Species

Homo sapiens

Symbol

rs1553868765

Category

Variant

Variant type

SNP

Overlaps

PRPF3

Location

1:150338154

Nucleotide Change

T>C

Most Severe Consequence

• splice region variant&intron variant

See all consequences

HGVS.g name

• NC_000001.11:g.150338154T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000324862.7:c.1036-6T>C
• ENSEMBL:ENST00000467329.5:n.1305-6T>C

Show All 10

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences