Variant #0000272353 (NC_000005.9:g.41155108G>A, NM_000065.2:c.2067C>T (C6))

Chromosome 5
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.41155108G>A
DNA change (hg38) g.41155006G>A
Published as C6(NM_000065.2):c.2067C>T (p.D689=), C6(NM_001115131.2):c.2067C>T (p.D689=)
ISCN -
DB-ID C6_000001 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) 0.00083 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-17 10:08:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C6 NM_000065.2 -/. - c.2067C>T r.(?) p.(Asp689=)


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