Variant #0001034010 (NC_000003.11:g.48602254C>T, NM_000094.3:c.8780G>A (COL7A1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48602254C>T
DNA change (hg38) -
Published as COL7A1(NM_000094.4):c.8780G>A (p.(Arg2927His))
ISCN -
DB-ID COL7A1_000361 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) 0.00018 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 2025-05-05 21:14:00 +02:00 (CEST)
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.8780G>A r.(?) p.(Arg2927His)
PFKFB4 NM_004567.2 +?/. - c.-8044G>A r.(?) p.(=)
UCN2 NM_033199.3 +?/. - c.-1131G>A r.(?) p.(=)


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