View genomic variant #0000000853

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.207011685G>A
Published as -
GERP 5.690
Segregation -
DB-ID NDUFS1_000006
MSCV MSCV_0000853
dbSNP ID NA
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS1 00000204 NM_001199981.1 0000000853 ./. - 7/18 c.571C>T p.(Pro191Ser) probably_damaging(0.998) missense_variant - deleterious(0)
NDUFS1 00000202 NM_001199982.1 0000000853 ./. - 5/16 c.346C>T p.(Pro116Ser) probably_damaging(0.998) missense_variant - deleterious(0)
NDUFS1 00000203 NM_001199983.1 0000000853 ./. - 7/18 c.508C>T p.(Pro170Ser) probably_damaging(0.998) missense_variant - deleterious(0)
NDUFS1 00000206 NM_001199984.1 0000000853 ./. - 8/19 c.721C>T p.(Pro241Ser) probably_damaging(0.998) missense_variant - deleterious(0)
NDUFS1 00000205 NM_005006.6 0000000853 ./. - 8/19 c.679C>T p.(Pro227Ser) probably_damaging(0.998) missense_variant - deleterious(0)
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None