Variant #0000281379 (NC_000006.11:g.34213296T>C, NM_178508.3:c.*995A>G (C6orf1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34213296T>C
DNA change (hg38) g.34245519T>C
Published as HMGA1(NM_145901.3):c.*635T>C
ISCN -
DB-ID HMGA1_000002
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) 0.99301 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMGA1 NM_145899.2 -/. - c.*635T>C r.(=) p.(=)
C6orf1 NM_178508.3 -/. - c.*995A>G r.(=) p.(=)


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