40370661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 80862040-A-G

40370721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80862099-C-T

40370744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80862129-G-A

40370801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80862159-A-T

40371433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80862677-C-G

40372567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80863726-A-G

40372726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80863876-G-T

40372895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 80864050-T-C

http://identifiers.org/hco/22/GRCh38#40372923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#80864078-C-A

40373171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80864313-G-C

40373251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80864396-G-T

40374921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80865772-A-T

40374978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80865832-G-A

40375015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80865871-C-T

40375103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80865952-A-G

40375573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80867360-T-A

40375573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80867360-T-C

http://identifiers.org/hco/22/GRCh38#40376223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#80867652-C-A

40387770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80873957-A-G

40387921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80874060-G-T

http://identifiers.org/hco/22/GRCh38#40388019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80874156-C-A

40388307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80874440-A-G

40388387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80874467-A-G

40388390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80874472-A-G

40391779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80880909-C-T

http://identifiers.org/hco/22/GRCh38#40391974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80880999-C-A

40391982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80881007-C-G

40391982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80881007-C-T

40392319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80881318-G-T

40392541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80881548-G-T

40392686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80881628-A-G

40396154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80883727-A-G

http://identifiers.org/hco/22/GRCh38#40396203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80883778-C-A

40397071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80884256-C-G

40397156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80884336-C-G

40398263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80884831-A-G

40398414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80884952-G-C

40400709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80886786-G-A

http://identifiers.org/hco/22/GRCh38#40400852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80886957-C-A

http://identifiers.org/hco/22/GRCh38#40400857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80886962-A-C

40400857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80886962-A-G

40400869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80886981-G-T

http://identifiers.org/hco/22/GRCh38#40400874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80886986-A-C

40400874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80886986-A-G

40400884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80886991-G-A

40400884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80886991-G-T

http://identifiers.org/hco/22/GRCh38#40400904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80887017-C-A

40400904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887017-C-T

40400931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887059-A-G

40401206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887298-G-C

40401339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887381-C-T

http://identifiers.org/hco/22/GRCh38#40401453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80887447-C-A

40401453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887447-C-G

40401453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887447-C-T

40401488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887471-T-C

http://identifiers.org/hco/22/GRCh38#40401494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80887477-C-A

40401494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887477-C-T

40401746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887719-G-T

http://identifiers.org/hco/22/GRCh38#40401769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80887742-A-C

40401769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887742-A-G

http://identifiers.org/hco/22/GRCh38#40401770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80887743-C-A

40402128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80887994-C-T

40402268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80888130-T-C

40402305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80888168-A-G

40403285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80889742-C-T

40403500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80889924-C-G

40403966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80890354-G-A

40403966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80890354-G-T

40403973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80890361-A-G

40404190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80890550-T-C

http://identifiers.org/hco/22/GRCh38#40404214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80890574-C-A

40404215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80890575-T-C

40404215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80890575-T-G

40404252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80890610-G-A

40404252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80890610-G-T

http://identifiers.org/hco/22/GRCh38#40404259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80890617-C-A

http://identifiers.org/hco/22/GRCh38#40404678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80891034-C-A

40404678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891034-C-T

http://identifiers.org/hco/22/GRCh38#40404694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80891050-C-A

40404694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891050-C-T

40404709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891069-G-A

40404709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891069-G-C

40404709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891069-G-T

40404747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891110-G-C

40404747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891110-G-T

40404908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891278-T-C

40404957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891443-T-A

http://identifiers.org/hco/22/GRCh38#40405004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80891490-C-A

40405004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891490-C-T

40405041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891529-A-G

40405041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891529-A-T

http://identifiers.org/hco/22/GRCh38#40405050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80891538-C-A

40405050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891538-C-T

40405062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891550-A-G

40405062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891550-A-T

http://identifiers.org/hco/22/GRCh38#40405357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80891856-C-A

40405357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891856-C-T

http://identifiers.org/hco/22/GRCh38#40405359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80891858-C-A

40405359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891858-C-G

40405359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891858-C-T

40405366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891865-G-A

40405366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891865-G-C

40405366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80891865-G-T

http://identifiers.org/hco/22/GRCh38#40405402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80891884-A-C

40405651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 80892054-G-A

40405780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80892183-C-T

40405837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80892240-T-C

40405837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80892240-T-G

40405910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892323-G-T

40405937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892350-G-A

http://identifiers.org/hco/22/GRCh38#40405968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80892389-C-A

40405968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892389-C-T

40406009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892418-T-G

40406017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892426-G-A

40406017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892426-G-T

40406075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80892487-C-T

40406088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80892500-G-T

40406145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80892557-C-G

40406145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80892557-C-T

http://identifiers.org/hco/22/GRCh38#40406263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80892706-C-A

40406263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892706-C-G

40406263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892706-C-T

40406318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892768-C-T

40406409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80892870-T-C

40406718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893130-A-G

40406747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893160-G-A

40406747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893160-G-T

40406926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893327-G-A

40406926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893327-G-C

40406926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893327-G-T

40407003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893411-T-C

http://identifiers.org/hco/22/GRCh38#40407033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80893441-C-A

40407033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80893441-C-T

40407046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80893454-G-A

40407046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80893454-G-T

40407124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893538-C-T

40407144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893562-T-G

40407160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893574-T-A

40407160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893574-T-C

40407160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893574-T-G

40407307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80893714-A-G

40407331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893738-G-A

40407393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893817-G-A

40407393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893817-G-T

http://identifiers.org/hco/22/GRCh38#40407394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80893818-C-A

40407394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80893818-C-T

http://identifiers.org/hco/22/GRCh38#40407410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80893832-C-A

40407410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80893832-C-T

40407576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80893998-G-A

40407604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894008-T-A

40407620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894014-G-A

40407620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894014-G-C

40407620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894014-G-T

40407621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894015-A-G

40407833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80894186-C-T

40407858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894211-C-G

40407858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894211-C-T

http://identifiers.org/hco/22/GRCh38#40407883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80894215-A-C

40407883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894215-A-G

40407883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894215-A-T

http://identifiers.org/hco/22/GRCh38#40408135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80894494-C-A

40408135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894494-C-G

40408135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894494-C-T

http://identifiers.org/hco/22/GRCh38#40408160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80894500-C-A

40408160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80894500-C-G

40408306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80894640-G-A

40408306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80894640-G-T

40408327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80894661-G-T

40408328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 80894662-C-T

40408405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80894739-C-T

40408458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894782-C-T

40408485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894809-C-T

40408510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894834-G-A

40408510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894834-G-T

40408593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894885-G-A

40408593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894885-G-C

40408608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894900-C-G

40408608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80894900-C-T

40408704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80894995-C-T

40408764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80895043-G-A

40408764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80895043-G-C

40408764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80895043-G-T

40408853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895116-C-G

40408860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895122-G-A

40408971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80895225-T-C

40408971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80895225-T-G

40409080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895300-G-A

40409080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895300-G-C

40409080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895300-G-T

40409090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895309-T-C

40409091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895310-A-G

40409120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80895342-A-G

40409192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80895385-G-A

40409192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80895385-G-C

40409192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80895385-G-T

40409862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896092-G-A

40409862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896092-G-T

40409902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896129-A-G

http://identifiers.org/hco/22/GRCh38#40409909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80896136-C-A

40409909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896136-C-T

40410006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896240-G-A

40410006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896240-G-C

40410006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896240-G-T

40410100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80896268-T-C

40410197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80896400-G-A

http://identifiers.org/hco/22/GRCh38#40410230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80896432-C-A

40410230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80896432-C-T

http://identifiers.org/hco/22/GRCh38#40410254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80896457-C-A

40410254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25228
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80896457-C-T