ClinVar

NM_006941.4(SOX10):c.1029C>G (p.Pro343=)

Genes:

POLR2F:RNA polymerase II, I and III subunit F [Gene - OMIM - HGNC]
SOX10:SRY-box transcription factor 10 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q13.1

Genomic location:

• Chr22: 37973867 (on Assembly GRCh38)
• Chr22: 38369874 (on Assembly GRCh37)

Preferred name:

NM_006941.4(SOX10):c.1029C>G (p.Pro343=)

HGVS:

• NC_000022.11:g.37973867G>C
• NG_007948.1:g.15666C>G
• NM_001301130.2:c.293+6697G>C
• NM_001301131.2:c.293+6697G>C
• NM_001363825.1:c.*38+1557G>C
• NM_006941.4:c.1029C>GMANE SELECT
• NP_008872.1:p.Pro343=
• NP_008872.1:p.Pro343=
• LRG_271t1:c.1029C>G
• LRG_271:g.15666C>G
• LRG_271p1:p.Pro343=
• NC_000022.10:g.38369874G>C
• NM_006941.3:c.1029C>G

This HGVS expression did not pass validation

Links:

dbSNP: rs1601879005

NCBI 1000 Genomes Browser:

rs1601879005

Molecular consequence:

• NM_001301130.2:c.293+6697G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001301131.2:c.293+6697G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001363825.1:c.*38+1557G>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_006941.4:c.1029C>G - synonymous variant - [Sequence Ontology: SO:0001819]