61162108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108181278-G-T

61162254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 108181184-T-C

http://identifiers.org/hco/5/GRCh38#61162380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#108181068-A-C

61162380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108181068-A-G

http://identifiers.org/hco/5/GRCh38#61162395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#108181058-A-C

61162395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108181058-A-G

61162435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108181028-T-A

61162435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108181028-T-C

61162435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108181028-T-G

61162519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 108180951-G-A

61162519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 108180951-G-C

61162519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 108180951-G-T

61162542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180926-A-G

61162555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180913-G-A

61162555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180913-G-T

61162569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108180909-G-A

61162569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108180909-G-C

http://identifiers.org/hco/5/GRCh38#61162579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#108180899-C-A

61162579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180899-C-T

61162602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180888-G-A

61162602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180888-G-T

http://identifiers.org/hco/5/GRCh38#61162624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#108180868-C-A

61162624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180868-C-T

61162671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180842-A-G

61162677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180836-C-G

61162679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180834-C-T

61162682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 108180831-G-T

61162934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108180684-G-A

61162998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108180634-G-T

http://identifiers.org/hco/5/GRCh38#61163072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108180570-A-C

61163255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108180387-T-C

61163689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108179943-A-G

http://identifiers.org/hco/5/GRCh38#61164454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108179562-C-A

61164520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108179493-A-G

61164558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108179472-G-C

61164644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108179392-C-G

61164644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108179392-C-T

61164656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108179373-A-G

61164694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108179344-T-C

61167293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108178482-A-G

61167439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108178350-C-G

61167517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 108178308-C-G

61167700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108178146-A-G

61167725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108178114-C-G

http://identifiers.org/hco/5/GRCh38#61167781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108178079-A-C

61167820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108178036-G-A

61167884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108177972-A-G

61167972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108177880-A-G

61168781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108176892-T-A

61168845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108176832-G-C

61169764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175889-T-C

61169830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175836-T-G

61169844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175816-C-T

61170098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175742-C-T

61170420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175396-T-C

61170489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175331-A-G

61170688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175137-T-C

61170769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108175061-T-C

61171494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108174402-G-A

61171511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108174393-C-G

61171511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108174393-C-T

61172362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108173660-A-G

http://identifiers.org/hco/5/GRCh38#61172829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108173295-A-C

61172842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108173282-T-C

61172897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108173231-C-T

http://identifiers.org/hco/5/GRCh38#61173036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108173098-C-A

61173270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108172885-G-A

61173477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108172683-C-T

61173506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108172654-T-C

61173752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108172437-C-T

61175195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108168810-C-T

61175563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108168483-C-T

61175775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108168252-C-T

61176350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108165054-T-C

61176680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108164672-G-A

61176721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108164541-G-T

61177472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108163777-G-T

61177550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108163701-A-G

61178172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162981-G-T

61178176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162977-A-T

61178294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162895-G-A

61178294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162895-G-T

61178410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162386-C-T

61178581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162233-T-C

61178600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162214-A-T

61178633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108162188-T-A

61178810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108161990-G-A

http://identifiers.org/hco/5/GRCh38#61179162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108161667-A-C

61179357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108161482-G-T

61179563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108161277-T-A

61179573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108161267-A-G

61179614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108161227-A-G

61179641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108161215-G-A

http://identifiers.org/hco/5/GRCh38#61179720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108161132-C-A

61179801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non coding transcript exon variant
orthologous variants: 108161068-C-T

61179954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108160914-A-G

61180366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non coding transcript exon variant
orthologous variants: 108160513-A-G

61180366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non coding transcript exon variant
orthologous variants: 108160513-A-T

61180389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non coding transcript exon variant
orthologous variants: 108160490-T-C

61180411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: non coding transcript exon variant
orthologous variants: 108160468-T-A

61180493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108160443-C-T

61180961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

61180961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

61181310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

61182403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108158738-T-A

http://identifiers.org/hco/5/GRCh38#61182711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108158467-A-C

61182711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108158467-A-T

61185276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108157319-C-G

61185287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108157308-G-A

61185400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108156856-A-G

http://identifiers.org/hco/5/GRCh38#61185405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108156851-C-A

61185622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108156624-G-A

61186159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108155924-A-G

61186359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108155754-C-T

61189835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108154598-T-C

61190175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108154300-G-A

61190381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108154148-A-G

61190454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108154088-C-G

61190531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108154010-G-A

61190640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108153902-T-G

61190678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108153864-T-C

61191256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108153305-G-A

http://identifiers.org/hco/5/GRCh38#61191320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108153232-C-A

http://identifiers.org/hco/5/GRCh38#61191854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108152559-C-A

61194500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108151695-C-G

http://identifiers.org/hco/5/GRCh38#61194653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108151370-A-C

61194667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108151356-A-T

61194675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108151348-A-T

61194697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108151331-C-T

61194728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108151315-A-T

61194737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108151306-A-G

61201307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108150996-G-T

61201381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108150941-A-G

http://identifiers.org/hco/5/GRCh38#61201504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108150777-C-A

61201504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108150777-C-G

61201533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108150689-T-G

61201749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150447-T-A

61201750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150446-G-A

61201764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150434-T-A

61201777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150421-T-G

61201844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150353-A-G

61201891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150310-A-G

61201917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150286-A-G

61201977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150226-G-C

61202117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150105-G-A

61202117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150105-G-T

61202129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150094-G-A

61202129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150094-G-C

61202182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108150041-A-G

61202296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108149928-C-T

61202677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108149520-T-C

61202689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108149507-A-G

61202724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108149452-G-T

61210532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142925-A-G

61210579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142879-G-A

61210579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142879-G-C

61210579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142879-G-T

61210850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142635-T-C

61211045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142431-A-T

61211071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142406-C-T

61211443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142062-T-A

61211443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108142062-T-G

61211581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108141881-A-G

61211624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108141840-A-T

http://identifiers.org/hco/5/GRCh38#61212064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108141436-A-C

61212171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108141339-A-G

61212174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108141336-A-G

61212326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108141192-A-G

61212606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108140913-C-T

61213853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108133785-C-T

61214276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108133386-A-G

61214488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108133171-T-G

61215119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132860-G-C

61215149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132830-G-T

61215200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132779-G-A

61215500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132512-G-C

61215513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132390-T-C

http://identifiers.org/hco/5/GRCh38#61215637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108132136-A-C

61215643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132130-A-G

61215697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132079-G-A

61215703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108132073-C-T

61215855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108131931-G-A

61215855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108131931-G-T

61215917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108131867-G-A

61215917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108131867-G-T

http://identifiers.org/hco/5/GRCh38#61215937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108131853-C-A

61215984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108131813-G-T

61216160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108131633-G-A

61216160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108131633-G-C

61216861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130965-G-T

61216953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130873-G-A

61216953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130873-G-T

61216998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130827-C-T

61217189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130653-G-C

61217267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130603-G-A

61217267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130603-G-C

61217267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130603-G-T

61217409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130468-A-G

61217623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130239-C-T

61217778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108130093-G-A

61217908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108129971-C-T

61218055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108129843-C-T

http://identifiers.org/hco/5/GRCh38#61218060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108129838-A-C

61218065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108129833-A-G

61218206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108129695-G-A

61218232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108129669-C-T

61219028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108128143-G-C

61219086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108128119-C-T

61220305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108126245-G-T

61220528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108126024-A-G

61220871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108125705-T-C

61221159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108125438-A-G

61221566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108125057-T-C

61221713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108124950-C-T

61221981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108124642-A-G

61222118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108124561-T-C

http://identifiers.org/hco/5/GRCh38#61222151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108124531-A-C

http://identifiers.org/hco/5/GRCh38#61222164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108124518-C-A

61227879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118536-A-G

61228047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118188-G-A

61228070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118165-T-A

61228070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118165-T-C

61228074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118161-T-A

61228074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118161-T-G

61228076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118159-A-T

61228142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108118123-A-G

61228348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117938-A-G

61228354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117932-G-A

http://identifiers.org/hco/5/GRCh38#61228497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108117837-A-C

61228539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117827-G-A

61228629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117731-A-G

61228777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117585-G-A

61229022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117339-T-G

http://identifiers.org/hco/5/GRCh38#61229265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108117128-C-A

61229265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117128-C-T

61229311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108117082-T-G

61229459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116960-C-T

61229580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116877-A-G

61229941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116566-T-A

61230168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116327-C-T

61230287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116211-G-A

61230449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116081-C-G

61230468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116070-T-A

http://identifiers.org/hco/5/GRCh38#61230478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108116060-C-A

61230478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116060-C-T

61230489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116047-T-C

61230500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108116036-G-A

61230926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108115839-A-G

61230930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108115835-T-C

61230958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108115809-G-A

61231084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108115488-C-T

61231911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 108114800-A-G

61231990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108114722-T-C

http://identifiers.org/hco/5/GRCh38#61232010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108114702-A-C

61232030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108114682-A-G