Yum, tasty mutations...

MutationTaster - study a chromosomal position

 MTQE documentation
NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 4 transcript(s)...
Querying Taster for transcript #1: ENST00000396634
Querying Taster for transcript #2: ENST00000376806
Querying Taster for transcript #3: ENST00000376802
Querying Taster for transcript #4: ENST00000376809
MT speed 0 s - this script 5.601137 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
HLA-Apolymorphism_automatic4.3319792197849e-12simple_aaeS129Psingle base exchangers1136700show file
HLA-Apolymorphism_automatic4.3319792197849e-12simple_aaeS129Psingle base exchangers1136700show file
HLA-Apolymorphism_automatic4.3319792197849e-12simple_aaeS129Psingle base exchangers1136700show file
HLA-Apolymorphism_automatic4.3319792197849e-12simple_aaeS129Psingle base exchangers1136700show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.999999999995668 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:29911086T>CN/A show variant in all transcripts   IGV
HGNC symbol HLA-A
Ensembl transcript ID ENST00000376806
Genbank transcript ID N/A
UniProt peptide P10314
alteration type single base exchange
alteration region CDS
DNA changes c.385T>C
cDNA.694T>C
g.2050T>C
AA changes S129P Score: 74 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 129
frameshift no
known variant Reference ID: rs1136700
databasehomozygous (C/C)heterozygousallele carriers
1000G24010361276
ExAC71571845325610
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
H3K79me2, Histone, Histone 3 Lysine 79 di-methylation
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
PolII, Polymerase, RNA Polymerase II
phyloP / phastCons
PhyloPPhastCons
(flanking)0.0740.055
-0.110.033
(flanking)2.2440.039
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 42
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      129TIQIMYGCDVGSDGRFLRGYRQDA
mutated  not conserved    129IMYGCDVGPDGRFLRGYRQD
Ptroglodytes  no homologue    
Mmulatta  not conserved  ENSMMUG00000029875  129TMYGCDLGPDGRLLRGYDQS
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
25308TOPO_DOMExtracellular (Potential).lost
115206REGIONAlpha-2.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1116 / 1116
position (AA) of stopcodon in wt / mu AA sequence 372 / 372
position of stopcodon in wt / mu cDNA 1425 / 1425
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 310 / 310
chromosome 6
strand 1
last intron/exon boundary 1421
theoretical NMD boundary in CDS 1061
length of CDS 1116
coding sequence (CDS) position 385
cDNA position
(for ins/del: last normal base / first normal base)		 694
gDNA position
(for ins/del: last normal base / first normal base)		 2050
chromosomal position
(for ins/del: last normal base / first normal base)		 29911086
original gDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered gDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
original cDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered cDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
wildtype AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGSD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWEL
SSQPTIPIVG IIAGLVLLGA VITGAVVAAV MWRRKSSGGE GVKDRKGGSY TQAASSDSAQ
GSDVSLTACK V*
mutated AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGPD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWEL
SSQPTIPIVG IIAGLVLLGA VITGAVVAAV MWRRKSSGGE GVKDRKGGSY TQAASSDSAQ
GSDVSLTACK V*
speed 1.11 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.999999999995668 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:29911086T>CN/A show variant in all transcripts   IGV
HGNC symbol HLA-A
Ensembl transcript ID ENST00000396634
Genbank transcript ID NM_002116
UniProt peptide P10314
alteration type single base exchange
alteration region CDS
DNA changes c.385T>C
cDNA.726T>C
g.2050T>C
AA changes S129P Score: 74 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 129
frameshift no
known variant Reference ID: rs1136700
databasehomozygous (C/C)heterozygousallele carriers
1000G24010361276
ExAC71571845325610
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
H3K79me2, Histone, Histone 3 Lysine 79 di-methylation
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
PolII, Polymerase, RNA Polymerase II
phyloP / phastCons
PhyloPPhastCons
(flanking)0.0740.055
-0.110.033
(flanking)2.2440.039
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 42
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      129TIQIMYGCDVGSDGRFLRGYRQDA
mutated  not conserved    129IMYGCDVGPDGRFLRGYRQD
Ptroglodytes  no homologue    
Mmulatta  not conserved  ENSMMUG00000029875  129TMYGCDLGPDGRLLRGYDQS
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
25308TOPO_DOMExtracellular (Potential).lost
115206REGIONAlpha-2.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1098 / 1098
position (AA) of stopcodon in wt / mu AA sequence 366 / 366
position of stopcodon in wt / mu cDNA 1439 / 1439
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 342 / 342
chromosome 6
strand 1
last intron/exon boundary 1435
theoretical NMD boundary in CDS 1043
length of CDS 1098
coding sequence (CDS) position 385
cDNA position
(for ins/del: last normal base / first normal base)		 726
gDNA position
(for ins/del: last normal base / first normal base)		 2050
chromosomal position
(for ins/del: last normal base / first normal base)		 29911086
original gDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered gDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
original cDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered cDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
wildtype AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGSD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWEL
SSQPTIPIVG IIAGLVLLGA VITGAVVAAV MWRRKSSDRK GGSYTQAASS DSAQGSDVSL
TACKV*
mutated AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGPD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWEL
SSQPTIPIVG IIAGLVLLGA VITGAVVAAV MWRRKSSDRK GGSYTQAASS DSAQGSDVSL
TACKV*
speed 1.09 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.999999999995668 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:29911086T>CN/A show variant in all transcripts   IGV
HGNC symbol HLA-A
Ensembl transcript ID ENST00000376802
Genbank transcript ID N/A
UniProt peptide P10314
alteration type single base exchange
alteration region CDS
DNA changes c.385T>C
cDNA.390T>C
g.2050T>C
AA changes S129P Score: 74 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 129
frameshift no
known variant Reference ID: rs1136700
databasehomozygous (C/C)heterozygousallele carriers
1000G24010361276
ExAC71571845325610
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
H3K79me2, Histone, Histone 3 Lysine 79 di-methylation
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
PolII, Polymerase, RNA Polymerase II
phyloP / phastCons
PhyloPPhastCons
(flanking)0.0740.055
-0.110.033
(flanking)2.2440.039
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 42
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      129TIQIMYGCDVGSDGRFLRGYRQDA
mutated  not conserved    129IMYGCDVGPDGRFLRGYRQD
Ptroglodytes  no homologue    
Mmulatta  not conserved  ENSMMUG00000029875  129TMYGCDLGPDGRLLRGYDQS
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
25308TOPO_DOMExtracellular (Potential).lost
115206REGIONAlpha-2.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 900 / 900
position (AA) of stopcodon in wt / mu AA sequence 300 / 300
position of stopcodon in wt / mu cDNA 905 / 905
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 6 / 6
chromosome 6
strand 1
last intron/exon boundary 901
theoretical NMD boundary in CDS 845
length of CDS 900
coding sequence (CDS) position 385
cDNA position
(for ins/del: last normal base / first normal base)		 390
gDNA position
(for ins/del: last normal base / first normal base)		 2050
chromosomal position
(for ins/del: last normal base / first normal base)		 29911086
original gDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered gDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
original cDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered cDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
wildtype AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGSD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWV*
mutated AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGPD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWV*
speed 1.19 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

polymorphism

 Model: simple_aae, prob: 0.999999999995668 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:29911086T>CN/A show variant in all transcripts   IGV
HGNC symbol HLA-A
Ensembl transcript ID ENST00000376809
Genbank transcript ID N/A
UniProt peptide P10314
alteration type single base exchange
alteration region CDS
DNA changes c.385T>C
cDNA.407T>C
g.2050T>C
AA changes S129P Score: 74 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 129
frameshift no
known variant Reference ID: rs1136700
databasehomozygous (C/C)heterozygousallele carriers
1000G24010361276
ExAC71571845325610
regulatory features DNase1, Open Chromatin, DNase1 Hypersensitive Site
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
H3K79me2, Histone, Histone 3 Lysine 79 di-methylation
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
PolII, Polymerase, RNA Polymerase II
phyloP / phastCons
PhyloPPhastCons
(flanking)0.0740.055
-0.110.033
(flanking)2.2440.039
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 42
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      129TIQIMYGCDVGSDGRFLRGYRQDA
mutated  not conserved    129IMYGCDVGPDGRFLRGYRQD
Ptroglodytes  no homologue    
Mmulatta  not conserved  ENSMMUG00000029875  129TMYGCDLGPDGRLLRGYDQS
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
25308TOPO_DOMExtracellular (Potential).lost
115206REGIONAlpha-2.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1098 / 1098
position (AA) of stopcodon in wt / mu AA sequence 366 / 366
position of stopcodon in wt / mu cDNA 1120 / 1120
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 23 / 23
chromosome 6
strand 1
last intron/exon boundary 1116
theoretical NMD boundary in CDS 1043
length of CDS 1098
coding sequence (CDS) position 385
cDNA position
(for ins/del: last normal base / first normal base)		 407
gDNA position
(for ins/del: last normal base / first normal base)		 2050
chromosomal position
(for ins/del: last normal base / first normal base)		 29911086
original gDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered gDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
original cDNA sequence snippet TGTATGGCTGCGACGTGGGGTCGGACGGGCGCTTCCTCCGC
altered cDNA sequence snippet TGTATGGCTGCGACGTGGGGCCGGACGGGCGCTTCCTCCGC
wildtype AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGSD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWEL
SSQPTIPIVG IIAGLVLLGA VITGAVVAAV MWRRKSSDRK GGSYTQAASS DSAQGSDVSL
TACKV*
mutated AA sequence MAVMAPRTLL LLLSGALALT QTWAGSHSMR YFFTSVSRPG RGEPRFIAVG YVDDTQFVRF
DSDAASQRME PRAPWIEQEG PEYWDQETRN VKAQSQTDRV DLGTLRGYYN QSEAGSHTIQ
IMYGCDVGPD GRFLRGYRQD AYDGKDYIAL NEDLRSWTAA DMAAQITKRK WEAAHEAEQL
RAYLDGTCVE WLRRYLENGK ETLQRTDPPK THMTHHPISD HEATLRCWAL GFYPAEITLT
WQRDGEDQTQ DTELVETRPA GDGTFQKWAA VVVPSGEEQR YTCHVQHEGL PKPLTLRWEL
SSQPTIPIVG IIAGLVLLGA VITGAVVAAV MWRRKSSDRK GGSYTQAASS DSAQGSDVSL
TACKV*
speed 1.19 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table

Problems