ClinVar

NM_000264.5(PTCH1):c.3422C>T (p.Ala1141Val)

Gene:

PTCH1:patched 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q22.32

Genomic location:

• Chr9: 95453505 (on Assembly GRCh38)
• Chr9: 98215787 (on Assembly GRCh37)

Preferred name:

NM_000264.5(PTCH1):c.3422C>T (p.Ala1141Val)

HGVS:

• NC_000009.12:g.95453505G>A
• NG_007664.1:g.68461C>T
• NM_000264.5:c.3422C>TMANE SELECT
• NM_001083602.3:c.3224C>T
• NM_001083603.3:c.3419C>T
• NM_001083604.3:c.2969C>T
• NM_001083605.3:c.2969C>T
• NM_001083606.3:c.2969C>T
• NM_001083607.3:c.2969C>T
• NM_001354918.2:c.3266C>T
• NP_000255.2:p.Ala1141Val
• NP_001077071.1:p.Ala1075Val
• NP_001077072.1:p.Ala1140Val
• NP_001077073.1:p.Ala990Val
• NP_001077074.1:p.Ala990Val
• NP_001077075.1:p.Ala990Val
• NP_001077076.1:p.Ala990Val
• NP_001341847.1:p.Ala1089Val
• LRG_515t1:c.3422C>T
• LRG_515:g.68461C>T
• NC_000009.11:g.98215787G>A
• NM_000264.3:c.3422C>T
• NR_149061.2:n.4161C>T

This HGVS expression did not pass validation

Protein change:

A1075V

Links:

dbSNP: rs376844749

NCBI 1000 Genomes Browser:

rs376844749

Molecular consequence:

• NM_000264.5:c.3422C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083602.3:c.3224C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083603.3:c.3419C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083604.3:c.2969C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083605.3:c.2969C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083606.3:c.2969C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083607.3:c.2969C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001354918.2:c.3266C>T - missense variant - [Sequence Ontology: SO:0001583]
• NR_149061.2:n.4161C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]