ClinVar

NM_006941.4(SOX10):c.231C>T (p.Ser77=)

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: 37983554 (on Assembly GRCh38)
• Chr22: 38379561 (on Assembly GRCh37)

Preferred name:

NM_006941.4(SOX10):c.231C>T (p.Ser77=)

HGVS:

• NC_000022.11:g.37983554G>A
• NG_007948.1:g.5979C>T
• NG_148296.1:g.831G>A
• NM_001301130.2:c.294-2600G>A
• NM_001301131.2:c.293+16384G>A
• NM_001363825.1:c.*38+11244G>A
• NM_006941.4:c.231C>TMANE SELECT
• NP_008872.1:p.Ser77=
• NP_008872.1:p.Ser77=
• LRG_271t1:c.231C>T
• LRG_271:g.5979C>T
• LRG_271p1:p.Ser77=
• NC_000022.10:g.38379561G>A
• NM_006941.3:c.231C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs377047321

NCBI 1000 Genomes Browser:

rs377047321

Molecular consequence:

• NM_001301130.2:c.294-2600G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001301131.2:c.293+16384G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001363825.1:c.*38+11244G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_006941.4:c.231C>T - synonymous variant - [Sequence Ontology: SO:0001819]