Variant #0000619951 (NC_000023.10:g.8536395T>C, NM_000216.2:c.1085A>G (KAL1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.8536395T>C
DNA change (hg38) g.8568354T>C
Published as ANOS1(NM_000216.3):c.1085A>G (p.E362G), ANOS1(NM_000216.4):c.1085A>G (p.E362G)
ISCN -
DB-ID KAL1_000033 See all 3 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) 1.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAL1 NM_000216.2 ?/. - c.1085A>G r.(?) p.(Glu362Gly)


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