ClinVar

NM_000264.5(PTCH1):c.3391G>A (p.Val1131Met)

Gene:

PTCH1:patched 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q22.32

Genomic location:

• Chr9: 95453536 (on Assembly GRCh38)
• Chr9: 98215818 (on Assembly GRCh37)

Preferred name:

NM_000264.5(PTCH1):c.3391G>A (p.Val1131Met)

HGVS:

• NC_000009.12:g.95453536C>T
• NG_007664.1:g.68430G>A
• NM_000264.5:c.3391G>AMANE SELECT
• NM_001083602.3:c.3193G>A
• NM_001083603.3:c.3388G>A
• NM_001083604.3:c.2938G>A
• NM_001083605.3:c.2938G>A
• NM_001083606.3:c.2938G>A
• NM_001083607.3:c.2938G>A
• NM_001354918.2:c.3235G>A
• NP_000255.2:p.Val1131Met
• NP_001077071.1:p.Val1065Met
• NP_001077072.1:p.Val1130Met
• NP_001077073.1:p.Val980Met
• NP_001077074.1:p.Val980Met
• NP_001077075.1:p.Val980Met
• NP_001077076.1:p.Val980Met
• NP_001341847.1:p.Val1079Met
• LRG_515t1:c.3391G>A
• LRG_515:g.68430G>A
• NC_000009.11:g.98215818C>T
• NM_000264.3:c.3391G>A
• NR_149061.2:n.4130G>A

This HGVS expression did not pass validation

Protein change:

V1065M

Links:

dbSNP: rs566619057

NCBI 1000 Genomes Browser:

rs566619057

Molecular consequence:

• NM_000264.5:c.3391G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083602.3:c.3193G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083603.3:c.3388G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083604.3:c.2938G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083605.3:c.2938G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083606.3:c.2938G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001083607.3:c.2938G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001354918.2:c.3235G>A - missense variant - [Sequence Ontology: SO:0001583]
• NR_149061.2:n.4130G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]