Variant #0000948186 (NC_000003.11:g.48637143C>T, NM_000094.3:c.-4551G>A (COL7A1))

Chromosome 3
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.48637143C>T
DNA change (hg38) -
Published as UQCRC1(NM_003365.2):c.1303G>A (p.(Glu435Lys)), UQCRC1(NM_003365.3):c.1303G>A (p.E435K)
ISCN -
DB-ID COL7A1_000566 See all 2 reported entries
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) 0.00158 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL7A1 NM_000094.3 -?/. - c.-4551G>A r.(?) p.(=)
UQCRC1 NM_003365.2 -?/. - c.1303G>A r.(?) p.(Glu435Lys)


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