ClinVar

NM_000264.5(PTCH1):c.3372A>T (p.Ala1124=)

Gene:

PTCH1:patched 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q22.32

Genomic location:

• Chr9: 95453555 (on Assembly GRCh38)
• Chr9: 98215837 (on Assembly GRCh37)

Preferred name:

NM_000264.5(PTCH1):c.3372A>T (p.Ala1124=)

HGVS:

• NC_000009.12:g.95453555T>A
• NG_007664.1:g.68411A>T
• NM_000264.5:c.3372A>TMANE SELECT
• NM_001083602.3:c.3174A>T
• NM_001083603.3:c.3369A>T
• NM_001083604.3:c.2919A>T
• NM_001083605.3:c.2919A>T
• NM_001083606.3:c.2919A>T
• NM_001083607.3:c.2919A>T
• NM_001354918.2:c.3216A>T
• NP_000255.2:p.Ala1124=
• NP_001077071.1:p.Ala1058=
• NP_001077072.1:p.Ala1123=
• NP_001077073.1:p.Ala973=
• NP_001077074.1:p.Ala973=
• NP_001077075.1:p.Ala973=
• NP_001077076.1:p.Ala973=
• NP_001341847.1:p.Ala1072=
• LRG_515t1:c.3372A>T
• LRG_515:g.68411A>T
• NC_000009.11:g.98215837T>A
• NM_000264.3:c.3372A>T
• NR_149061.2:n.4111A>T

This HGVS expression did not pass validation

Links:

dbSNP: rs756638660

NCBI 1000 Genomes Browser:

rs756638660

Molecular consequence:

• NR_149061.2:n.4111A>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000264.5:c.3372A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083602.3:c.3174A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083603.3:c.3369A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083604.3:c.2919A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083605.3:c.2919A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083606.3:c.2919A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083607.3:c.2919A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001354918.2:c.3216A>T - synonymous variant - [Sequence Ontology: SO:0001819]