Variant #0000548668 (NC_000012.11:g.56105932A>C, NM_002905.3:c.-8402A>C (RDH5))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56105932A>C
DNA change (hg38) g.55712148A>C
Published as ITGA7(NM_001144997.1):c.14-14T>G (p.(=))
ISCN -
DB-ID BLOC1S1_000012
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01518 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLOC1S1 NM_001487.3 -?/. - c.-3904A>C r.(?) p.(=)
ITGA7 NM_002206.2 -?/. - c.-4466T>G r.(?) p.(=)
RDH5 NM_002905.3 -?/. - c.-8402A>C r.(?) p.(=)
METTL7B NM_152637.2 -?/. - c.*28099A>C r.(=) p.(=)


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