ClinVar

NM_000264.5(PTCH1):c.3375C>T (p.Pro1125=)

Gene:

PTCH1:patched 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q22.32

Genomic location:

• Chr9: 95453552 (on Assembly GRCh38)
• Chr9: 98215834 (on Assembly GRCh37)

Preferred name:

NM_000264.5(PTCH1):c.3375C>T (p.Pro1125=)

HGVS:

• NC_000009.12:g.95453552G>A
• NG_007664.1:g.68414C>T
• NM_000264.4:c.3375C>T
• NM_000264.5:c.3375C>TMANE SELECT
• NM_001083602.3:c.3177C>T
• NM_001083603.3:c.3372C>T
• NM_001083604.3:c.2922C>T
• NM_001083605.3:c.2922C>T
• NM_001083606.3:c.2922C>T
• NM_001083607.3:c.2922C>T
• NM_001354918.2:c.3219C>T
• NP_000255.2:p.Pro1125=
• NP_001077071.1:p.Pro1059=
• NP_001077072.1:p.Pro1124=
• NP_001077073.1:p.Pro974=
• NP_001077074.1:p.Pro974=
• NP_001077075.1:p.Pro974=
• NP_001077076.1:p.Pro974=
• NP_001341847.1:p.Pro1073=
• LRG_515t1:c.3375C>T
• LRG_515:g.68414C>T
• NC_000009.11:g.98215834G>A
• NM_000264.3:c.3375C>T
• NR_149061.2:n.4114C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs369760318

NCBI 1000 Genomes Browser:

rs369760318

Molecular consequence:

• NR_149061.2:n.4114C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000264.5:c.3375C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083602.3:c.3177C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083603.3:c.3372C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083604.3:c.2922C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083605.3:c.2922C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083606.3:c.2922C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001083607.3:c.2922C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001354918.2:c.3219C>T - synonymous variant - [Sequence Ontology: SO:0001819]