ClinVar

NM_133509.5(RAD51B):c.1036+44868T>C

Gene:

RAD51B:RAD51 paralog B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q24.1

Genomic location:

• Chr14: 68513118 (on Assembly GRCh38)
• Chr14: 68979835 (on Assembly GRCh37)

Preferred name:

NM_133509.5(RAD51B):c.1036+44868T>C

HGVS:

• NC_000014.9:g.68513118T>C
• NG_023267.2:g.698340T>C
• NM_001321809.2:c.1036+44868T>C
• NM_001321810.2:c.1036+44868T>C
• NM_001321812.1:c.1037-27082T>C
• NM_001321814.2:c.1037-27082T>C
• NM_001321815.1:c.922+44868T>C
• NM_001321818.2:c.1036+44868T>C
• NM_001321821.2:c.1036+44868T>C
• NM_133509.5:c.1036+44868T>C
• NC_000014.8:g.68979835T>C

This HGVS expression did not pass validation

Links:

dbSNP: rs11624333

NCBI 1000 Genomes Browser:

rs11624333

Molecular consequence:

• NM_001321809.2:c.1036+44868T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001321810.2:c.1036+44868T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001321812.1:c.1037-27082T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001321814.2:c.1037-27082T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001321815.1:c.922+44868T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001321818.2:c.1036+44868T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001321821.2:c.1036+44868T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_133509.5:c.1036+44868T>C - intron variant - [Sequence Ontology: SO:0001627]