Variant #0000526605 (NC_000006.11:g.108197892_108197893dup, NC_000006.11(NM_007214.4):c.1936-10_1936-9dup (SEC63))

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.108197892_108197893dup
DNA change (hg38) g.107876688_107876689dup
Published as SEC63(NM_007214.4):c.1936-10_1936-9dupTT, SEC63(NM_007214.5):c.1936-10_1936-9dupTT, SEC63(NM_007214.5):c.1936-11_1936-10dupTT
ISCN -
DB-ID SEC63_000021 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
SEC63 NM_007214.4 -/. - c.1936-10_1936-9dup r.(=) p.(=)


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