52169651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246303-G-T

http://identifiers.org/hco/12/GRCh38#52169708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101246360-A-C

52169932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246571-T-A

52169932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246571-T-C

52169994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246634-G-T

52170001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246641-G-A

52170001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246641-G-T

52170019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246662-G-A

52170019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246662-G-C

52170019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246662-G-T

52170180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246801-G-A

52170180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246801-G-T

52170266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246886-G-T

52170295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246915-T-G

52170343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246928-G-A

52170343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246928-G-C

52170343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246928-G-T

52170375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246934-A-G

52170375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246934-A-T

http://identifiers.org/hco/12/GRCh38#52170411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101246959-C-A

52170411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246959-C-T

52170436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246984-G-A

52170436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101246984-G-T

http://identifiers.org/hco/12/GRCh38#52170533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247066-C-A

http://identifiers.org/hco/12/GRCh38#52170632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247155-C-A

52170632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247155-C-T

52170652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247174-G-A

52170839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247289-G-A

52170839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247289-G-T

52170855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247305-A-G

http://identifiers.org/hco/12/GRCh38#52170887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247332-C-A

52170887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247332-C-T

52170935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247376-C-T

52170965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247409-G-A

52171021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247466-A-G

52171021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247466-A-T

http://identifiers.org/hco/12/GRCh38#52171070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247510-C-A

52171070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247510-C-T

52171077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247517-A-G

52171124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247556-T-C

52171219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247635-G-A

52171219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247635-G-T

52171278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247689-A-G

52171278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101247689-A-T

http://identifiers.org/hco/12/GRCh38#52171305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101247706-C-A

52171404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101247802-T-C

52171557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101247953-G-A

52171587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101247982-G-C

52171617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101248010-A-T

http://identifiers.org/hco/12/GRCh38#52171704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101248096-C-A

52171704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101248096-C-T

52171837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101248241-G-A

52171837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101248241-G-T

http://identifiers.org/hco/12/GRCh38#52172165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#101248855-C-A

52172165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101248855-C-T

52172343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249022-G-A

52172343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101249022-G-T

52172362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249041-G-A

52172469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249132-G-A

52172469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249132-G-T

52172489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249151-G-A

52172489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249151-G-C

52172489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249151-G-T

52172565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249199-C-T

52172730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249287-C-T

52172777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249329-C-G

52172787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249340-G-C

http://identifiers.org/hco/12/GRCh38#52172898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249423-C-A

52172927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249449-T-C

52172943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249465-G-A

52172943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249465-G-T

http://identifiers.org/hco/12/GRCh38#52172946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249468-C-A

52172946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249468-C-T

52172969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249490-T-C

52172980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249501-T-C

52172985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249504-G-A

52172985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249504-G-C

52172985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249504-G-T

52172994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249513-C-T

52172996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249515-T-C

52173050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249567-A-G

52173050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249567-A-T

http://identifiers.org/hco/12/GRCh38#52173068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249585-C-A

52173071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249588-C-T

52173137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249654-G-A

52173137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249654-G-C

52173140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101249657-C-T

52173190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249709-G-A

52173190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249709-G-T

http://identifiers.org/hco/12/GRCh38#52173211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249743-C-A

52173211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249743-C-G

52173211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249743-C-T

http://identifiers.org/hco/12/GRCh38#52173225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249756-C-A

52173225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249756-C-T

http://identifiers.org/hco/12/GRCh38#52173255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249784-C-A

http://identifiers.org/hco/12/GRCh38#52173277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249829-C-A

52173277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249829-C-G

52173277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249829-C-T

http://identifiers.org/hco/12/GRCh38#52173278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249830-C-A

52173278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249830-C-T

http://identifiers.org/hco/12/GRCh38#52173283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249835-C-A

52173283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249835-C-G

52173331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249880-C-T

52173332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249881-T-C

52173415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249935-T-C

http://identifiers.org/hco/12/GRCh38#52173474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249975-C-A

52173474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249975-C-T

52173476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249977-T-A

52173476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249977-T-G

http://identifiers.org/hco/12/GRCh38#52173481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101249980-C-A

52173481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249980-C-G

52173481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101249980-C-T

http://identifiers.org/hco/12/GRCh38#52173520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101250017-C-A

52173520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250017-C-G

52173520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250017-C-T

52173543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250040-C-T

52173668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101250126-C-T

52173746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101250204-C-T

52173787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250246-G-A

52173787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250246-G-T

52174012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250406-A-G

52174580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250789-C-T

52174581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250790-G-A

52174592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101250794-T-C

52175001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251168-G-A

52175176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251345-G-A

52175439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251544-G-A

52175465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101251567-C-T

52175949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252006-T-G

52176013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252066-A-T

52176209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252273-C-T

52176210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252274-G-A

52176287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252335-G-T

52176354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101252417-G-A

52178794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255202-C-T

http://identifiers.org/hco/12/GRCh38#52178886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101255301-C-A

52178905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255317-G-A

52179383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255630-G-C

http://identifiers.org/hco/12/GRCh38#52179600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101255789-C-A

52179613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101255794-C-G

52179996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256179-C-T

52180037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256222-C-G

52180037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256222-C-T

52180385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256477-G-A

52180385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256477-G-T

52180422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256505-G-C

52180422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101256505-G-T

52180654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101256669-T-C

52180693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101256698-G-A

52180789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101256783-G-A

52180849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101257305-A-G

52180861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101257326-G-A

52180861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101257326-G-C

52180861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101257326-G-T

52180892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101257352-G-A

52181008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257461-T-A

52181008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257461-T-C

52181060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257508-T-A

52181243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101257743-C-G

52181878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101258385-T-C

52181985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101258481-C-T

52182251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101258707-T-A

52183004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260099-G-A

52183064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260154-A-G

52183069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260159-A-G

http://identifiers.org/hco/12/GRCh38#52183397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101260472-C-A

52183397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260472-C-T

52184015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101260849-G-T

52184190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261013-G-A

52184190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261013-G-T

52184604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261371-C-T

52184640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261401-A-G

52184871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261638-T-C

52184965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261715-C-T

52185051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261808-T-C

52185163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261904-G-T

52185252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261966-A-G

52185280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101261994-A-G

52185380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101262092-T-C

52185459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101262171-C-T

52185531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101262243-C-T

52185534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 101262246-C-T

http://identifiers.org/hco/12/GRCh38#52185647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101262352-C-A

52185647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101262352-C-G

52185647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101262352-C-T

52185653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101262358-G-C

52185740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101262452-T-C

52185814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101262521-A-G

52186049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101262729-C-T

52186183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101263643-C-G

52187772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264160-G-C

52187772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264160-G-T

52187827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264214-C-G

52187827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264214-C-T

52187887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264274-G-A

52188262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264604-G-A

52188605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101264974-A-G

52188934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265271-C-T

52188972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265288-C-T

52189115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265431-G-C

52189117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101265433-T-G

52190017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266190-C-T

52190150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266262-G-A

52190506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266682-G-A

52190626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266754-T-C

52190676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101266797-A-G

52191111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267171-G-A

52191113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267173-A-G

52191123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267183-C-T

52191249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267325-G-A

52191249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267325-G-T

52191278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267351-C-T

http://identifiers.org/hco/12/GRCh38#52191566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101267597-C-A

52191566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101267597-C-T

52191903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101267936-G-A

52191903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101267936-G-T

http://identifiers.org/hco/12/GRCh38#52191971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#101268006-C-A

52191971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101268006-C-G

52191971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27056
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101268006-C-T