http://identifiers.org/hco/2/GRCh38#6918169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26464731-C-A

6918169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26464731-C-T

6918230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26464674-T-C

http://identifiers.org/hco/2/GRCh38#6918252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26464651-C-A

6918252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26464651-C-G

6918252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26464651-C-T

http://identifiers.org/hco/2/GRCh38#6918285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26464608-C-A

6918285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26464608-C-T

http://identifiers.org/hco/2/GRCh38#6918358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26464534-C-A

6919484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26463829-G-A

6919955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26463126-T-G

6920110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462971-C-T

6920192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26462888-C-T

6920463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462650-A-G

6920481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462637-G-A

6920564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462567-C-G

6920569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462562-T-C

6920588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462547-C-T

6920621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462523-G-C

6921040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462162-C-T

6921057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26462146-C-G

6921362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26461692-C-T

6921483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26461570-G-A

6922013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26461165-A-G

6922022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26461156-A-G

6922022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26461156-A-T

6922450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26460415-A-G

6922452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26460413-A-G

6922501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26460364-G-A

6923259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26459848-T-G

6923651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26459453-A-T

6923708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26459380-A-G

6923743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26459338-C-T

6923961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26459084-G-T

6924230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458817-C-T

6924244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458803-C-T

http://identifiers.org/hco/2/GRCh38#6924552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26458530-C-A

6924552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458530-C-T

6924553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458529-G-A

6924553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458529-G-T

6924625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458466-G-T

6925027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458155-C-T

6925161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26458039-A-G

6925208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457991-C-T

6925217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457983-G-A

6925275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457942-C-G

6925275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457942-C-T

6925326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457906-A-G

6925332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457900-G-A

6925501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457771-G-A

6925501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26457771-G-C

http://identifiers.org/hco/2/GRCh38#6925608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26457685-A-C

6925863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

6925904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

6925932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

6926030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456910-T-G

6926103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456852-C-G

http://identifiers.org/hco/2/GRCh38#6926161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26456797-C-A

6926315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456335-C-T

6926379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456272-G-A

6926431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456234-G-A

6926529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456137-G-A

6926547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456119-G-T

6926580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456089-A-G

6926580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456089-A-T

6926688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26456023-C-T

6926725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26455994-C-T

http://identifiers.org/hco/2/GRCh38#6926748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26455971-A-C

6927082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26455684-C-G

6927404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26455388-C-G

http://identifiers.org/hco/2/GRCh38#6927476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26455320-C-A

6927476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26455320-C-T

6927549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26455252-G-A

6927738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26455087-A-G

6928591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26453906-C-T

6928693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26453808-T-A

6929173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26453378-C-G

6929195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26453358-T-C

http://identifiers.org/hco/2/GRCh38#6929313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26453260-C-A

http://identifiers.org/hco/2/GRCh38#6929628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26452658-A-C

6929775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26452506-G-A

6929775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26452506-G-T

http://identifiers.org/hco/2/GRCh38#6929867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26452409-C-A

6929867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26452409-C-G

6929914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26452365-G-A

6929914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26452365-G-C

6931375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26448551-A-G

6931421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26448491-A-G

6931475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26448441-A-G

http://identifiers.org/hco/2/GRCh38#6931504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26448414-A-C

6931847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26447908-T-G

6932093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26447692-T-A

6932093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26447692-T-C

6932093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26447692-T-G

6932094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26447691-C-G

6932143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26447645-T-A

http://identifiers.org/hco/2/GRCh38#6932144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26447644-C-A

6932144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26447644-C-T

6932461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26445608-T-A

6932619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26445448-T-G

6932933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26445151-T-C

6933056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26445014-C-T

6933144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26444924-A-G

6933219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26444842-A-G

6933306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26444761-T-C

6933312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26444748-A-G

6933773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26444427-G-A

6933861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26444343-A-G

6936524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26443045-C-G

6936596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442994-A-G

6936654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442945-C-T

6936658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442941-A-T

6936743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442878-T-G

6936748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26442873-T-C

6937448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26441711-A-G

6937449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26441710-T-C

6937583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26441572-A-G

http://identifiers.org/hco/2/GRCh38#6937997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26441213-A-C

6938056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26441165-G-A

http://identifiers.org/hco/2/GRCh38#6938059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26441162-C-A

6938231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26440978-C-T

6938256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26440953-T-C

6938256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26440953-T-G

http://identifiers.org/hco/2/GRCh38#6940923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26439599-C-A

6940923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439599-C-G

6940923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439599-C-T

6940942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26439578-T-C

6941023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26439497-T-C

http://identifiers.org/hco/2/GRCh38#6941038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26439485-C-A

6941064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26439474-G-T

6941066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26439472-C-T

6941075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26439463-G-T

6941093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26439445-A-G

6941175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439363-T-C

6941212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439322-A-G

6941223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439316-G-C

6941223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439316-G-T

6941288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439249-T-C

6941313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439224-A-G

6941333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439201-C-T

6941401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439079-T-G

http://identifiers.org/hco/2/GRCh38#6941460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26439027-A-C

6941473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26439014-G-A

6941587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438906-G-A

http://identifiers.org/hco/2/GRCh38#6941595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26438898-C-A

6941656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438846-T-C

6941680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438822-A-T

6941684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438818-T-C

6941700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438808-G-A

6941723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438787-T-A

6941723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438787-T-C

6941910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438579-G-A

http://identifiers.org/hco/2/GRCh38#6941912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26438577-C-A

6941912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438577-C-T

6941915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438574-G-A

6941940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438549-G-A

6941986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438518-G-C

6942017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438480-A-G

6942044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438453-C-G

6942071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438426-G-A

6943056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26438129-G-C

6943281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26437912-C-G

6943282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26437911-C-G

6943295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26437896-G-A

6943411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26437734-G-A

6944209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436940-C-T

6944413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436728-G-T

6944414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436727-C-T

6944776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26436376-T-G

6945105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26435990-G-A

6945138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26435957-C-T

6955003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430920-T-A

6955003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430920-T-G

http://identifiers.org/hco/2/GRCh38#6955146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26430801-A-C

6955187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430750-G-A

6955220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430712-G-A

6955286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430649-A-G

6955375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430548-C-G

6955505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430416-C-G

6955505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430416-C-T

6955668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430174-T-A

6955729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430042-C-T

6956056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429724-A-G

6956366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429411-A-G

6956424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429359-C-T

6956480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429300-A-G

6956521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429276-C-G

6956626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429179-G-C

6956672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429149-G-T

6956751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429071-G-A

6956751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429071-G-T

6957580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428204-C-T

6957610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428187-C-G

6957610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428187-C-T

6957737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428071-A-G

6958025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427803-G-A

6958033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427795-G-A

http://identifiers.org/hco/2/GRCh38#6958075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26427752-A-C

6958075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427752-A-G

6958165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427680-C-G

6958214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427631-T-C

6958220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427625-C-T

6959105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26426071-A-G

6959106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26426070-G-C

6959192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26426000-A-G

6959252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425949-C-G

6959264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425937-T-C

6959302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425899-G-A

6959303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425898-C-G

6959317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425886-G-A

6959350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425852-T-C

6959889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425724-A-G

6959903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425710-C-T

6959939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425675-C-T

6959993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425634-T-C

6959999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425628-T-C

6960019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425610-G-A

6960084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425534-C-T

6960098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26425520-G-A

6960835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424256-G-C

6960870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424211-C-G

6960940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424154-G-A

6960968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424123-G-A

6960968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424123-G-T

6960979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424108-C-T

6961074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424017-A-G

6961075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26424016-T-C

6961231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26423860-T-A

6961240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26423851-T-G

6961420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26423688-C-G

http://identifiers.org/hco/2/GRCh38#6961431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26423666-C-A

6961462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26423646-G-A

6961488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26423620-C-T

6961546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26423561-A-G

6961741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26423385-C-T

6967673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26421045-G-T

6967732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26420984-T-C

6967756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26420959-C-G

6967795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26420926-A-G

6967827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26420899-T-A

6967827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26420899-T-C

6967857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26420865-G-C

6967883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26420830-T-C

http://identifiers.org/hco/2/GRCh38#6968408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26420259-C-A

6968922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26419759-C-T

6969058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26419607-C-G

6969183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26419478-A-G

6969251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26419402-C-T

6969263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26419399-G-A

6970823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26418948-G-A

6970823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26418948-G-T

6970834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26418937-G-A

6972016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26416691-T-C

6972232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26416497-C-T

6972411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26416324-C-T

6972984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415711-C-G

6973015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415681-G-A

6973040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415656-G-A

6973200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415517-C-T

6973210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415507-G-A

6973210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415507-G-T

6973222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415495-T-C

6973402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415352-T-C

6973460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415326-G-T

6973757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26415040-A-T

6974572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26413321-A-G

6974572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26413321-A-T

http://identifiers.org/hco/2/GRCh38#6974606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26413288-A-C

6975469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26411690-T-C

6977078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26410201-G-A

6977078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26410201-G-T

6977239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26410060-C-T

6977726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26409790-T-C

6977907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26409660-G-A

6977907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26409660-G-C

6978724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26408971-T-C

6978851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408849-G-A

6978851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408849-G-T

6978947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408783-A-G

http://identifiers.org/hco/2/GRCh38#6978974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26408751-C-A

6978974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408751-C-G

6979032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408694-G-T

6979046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408680-A-T

6979080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408647-C-T

6979082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408645-T-C

6979117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408637-G-A

6979142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408618-G-T

6979167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408594-G-A

6979167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408594-G-T

6979209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408555-T-C

6979209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408555-T-G

6979247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408521-A-T

6979306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408471-T-C

6979331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408446-C-T

6979401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408379-T-C

6979442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408351-A-G

6979482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26408311-G-A

6982318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26407182-T-G

6982446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26407077-T-A

6982569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26406947-C-T

6982729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26406797-T-C

6982842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26406685-G-A

6983638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26406419-T-A

6983638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26406419-T-C

6983678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26406380-A-G

6986212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401744-C-G

6986212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401744-C-T

http://identifiers.org/hco/2/GRCh38#6986245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26401714-A-C

6986300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401663-T-G

6986363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401604-C-G

6986365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401602-C-T

6986425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401543-C-T

6986427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401541-G-C

6986499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401487-A-G

6986928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26401109-T-G

6988209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

6988504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/2/GRCh38#6988507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

6988507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

6989045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

6989165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/2/GRCh38#6992391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26393898-C-A

6992411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393885-G-A

6992555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393746-C-G

6992611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393697-G-T

6992772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393575-C-T

6992934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393417-C-T

6992936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393415-G-A

6993143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393139-T-G

6993263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26393023-T-C

6993296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392985-A-G

6993455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392854-G-C

6993505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392808-C-T

6993625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392674-C-T

http://identifiers.org/hco/2/GRCh38#6993664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26392635-A-C

6993713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392598-T-G

6993932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392421-C-G

6994013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392361-G-A

6994053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392340-A-T

6994217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26392194-C-T

6994445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391963-A-G

6994507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391912-A-T

6994525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391897-A-G

6994547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391875-A-G

6994639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391709-C-T

6994820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391512-G-A

6994965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391354-C-T

6994993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391326-G-A

6994993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391326-G-T

6995172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26391202-G-A

http://identifiers.org/hco/2/GRCh38#6996797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26389573-C-A

6996797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26389573-C-T

http://identifiers.org/hco/2/GRCh38#6996831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26389534-C-A

6996844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26389521-G-T

6996858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26389502-G-A

6996858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26389502-G-T

6997029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26389335-A-G

6997083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26389281-A-G

6997083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26389281-A-T

http://identifiers.org/hco/2/GRCh38#6997201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26389191-C-A

6997201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26389191-C-G

http://identifiers.org/hco/2/GRCh38#6997357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26389042-A-C

6997357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26389042-A-G

6997448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26388953-G-A

6997499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26388903-T-C

http://identifiers.org/hco/2/GRCh38#6998617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26387290-A-C

6998641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387266-A-G

6998713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387185-A-G

6998962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26386952-G-A

6998962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26386952-G-C

6999302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26386637-G-A

6999343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26386597-G-A

6999397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26386541-G-A

7005066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385637-G-C

http://identifiers.org/hco/2/GRCh38#7005083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26385620-A-C

7005382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385349-G-A

7005382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385349-G-C

7005393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385339-C-T

7006189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26384081-G-A

7006320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383974-T-A

7006461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383894-G-A

7006741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383630-G-T

7006747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383624-T-C

7006833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383601-A-T

7007035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383422-C-T

7007271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383186-T-C

http://identifiers.org/hco/2/GRCh38#7007322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26383135-C-A

7007322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383135-C-T

7007357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383121-C-T

http://identifiers.org/hco/2/GRCh38#7007372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26383106-C-A

7010171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26381622-G-A

7010719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26381133-T-G

7010721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26381131-A-G

7010721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26381131-A-T

7010740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26381113-G-T

7010810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26381049-C-T

7010820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26381039-C-G

http://identifiers.org/hco/2/GRCh38#7011520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26379916-A-C

7011553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379884-A-T

7012106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379255-A-G

7012746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26378709-G-A

7014593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377458-T-C

7014633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26377423-G-A

7014633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26377423-G-T

7014693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377356-G-A

7014812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377235-T-C

7014812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377235-T-G

7014818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377232-A-T

7014837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377212-G-A

7014855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377194-A-T

7014939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377123-C-T

7015032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377032-G-A

7015032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377032-G-C

7015228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376854-G-A

7015629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376478-A-G

7015629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376478-A-T

7015732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376386-C-T

7015771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376349-A-G

7015798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376323-C-T

7015843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376273-G-C

7015852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376268-C-G

7016291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375667-G-A

7016324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375634-G-A

7016591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375374-A-T

7016607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375358-G-T

7016756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375220-T-G

7017047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374951-A-G

7017074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374924-G-A

http://identifiers.org/hco/2/GRCh38#7017340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26374785-A-C

http://identifiers.org/hco/2/GRCh38#7017343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26374778-C-A

7017343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374778-C-G

7017343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374778-C-T

7017478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374661-G-A

7017523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374611-G-A

7017740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374368-T-C

7017845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374093-T-G

7018136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373843-T-C

7018142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373837-C-T

7018393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373573-C-G

7018445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373522-A-T

7018459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373508-C-T

7018886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373153-T-G

7018967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373075-G-A

7019084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26372958-C-G

7019237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26372806-C-T

http://identifiers.org/hco/2/GRCh38#7019270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26372765-A-C

http://identifiers.org/hco/2/GRCh38#7019407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26372425-A-C

7019476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26372368-C-G

7019476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26372368-C-T

http://identifiers.org/hco/2/GRCh38#7019704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26372138-A-C

7020290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371383-A-G

7020344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371329-G-T

http://identifiers.org/hco/2/GRCh38#7020373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26371304-C-A

7020373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371304-C-T

http://identifiers.org/hco/2/GRCh38#7020388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26371289-C-A

7020388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371289-C-T

http://identifiers.org/hco/2/GRCh38#7020427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26371216-C-A

7020427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371216-C-T

http://identifiers.org/hco/2/GRCh38#7020431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26371212-C-A

7020622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26371007-C-T

7020690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26370943-G-T

7020728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26370873-G-T

http://identifiers.org/hco/2/GRCh38#7020749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26370853-C-A

http://identifiers.org/hco/2/GRCh38#7020786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26370816-A-C

http://identifiers.org/hco/2/GRCh38#7020789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26370813-C-A

7020980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370695-G-C

7021060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370617-G-A

7021088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370528-A-G

7021136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370470-C-T

7021157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370449-T-C

7021304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370317-G-C

7021356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370280-G-C

http://identifiers.org/hco/2/GRCh38#7021376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26370260-C-A

7021436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370222-T-C

http://identifiers.org/hco/2/GRCh38#7021485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26370174-C-A

7021485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370174-C-T

7021563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370123-T-G

7021579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370107-G-A

7021641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370048-G-C

7021643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370046-G-T

7021671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370017-A-G

7023248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369176-G-T

http://identifiers.org/hco/2/GRCh38#7023742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26368307-A-C

7023925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26368144-G-C

7023973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26368102-A-G

7024191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367954-T-C

7024205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367943-C-T

http://identifiers.org/hco/2/GRCh38#7024250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26367909-C-A

7024250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367909-C-G

7024250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367909-C-T

7024272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367885-G-T

7024284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367873-G-T

7024285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367872-A-T

7024286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367871-G-A

7024286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367871-G-T

7024335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367824-T-C

7024397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26367765-G-A

7024397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26367765-G-C

7024545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367619-G-A

http://identifiers.org/hco/2/GRCh38#7024547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26367617-C-A

7024547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367617-C-T

7024609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367560-T-A

7024609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367560-T-G

7024631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367541-G-A

7024631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367541-G-T

http://identifiers.org/hco/2/GRCh38#7024640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26367532-C-A

7024640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367532-C-T

http://identifiers.org/hco/2/GRCh38#7028903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26365141-A-C

7029198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364905-A-T

7029236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364868-C-T

7029478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364623-G-T

7029497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364600-T-A

7029618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364477-G-A

http://identifiers.org/hco/2/GRCh38#7030019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26364209-C-A

7030019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364209-C-T

http://identifiers.org/hco/2/GRCh38#7030021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26364207-C-A

7030021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364207-C-T

http://identifiers.org/hco/2/GRCh38#7030027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26364201-A-C

7030065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364169-A-G

7030065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364169-A-T

7030099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364133-T-C

http://identifiers.org/hco/2/GRCh38#7030111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26364121-C-A

7030263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26363958-G-A

7030263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26363958-G-C

7030289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26363910-G-A

7030317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26363883-T-G

7037190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362494-G-A

7037244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362449-G-T

7037252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362441-G-A

7037334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362361-A-T

7037565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362004-G-A

7037902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26361761-G-C

7038040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26361641-T-G

7038198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361515-G-A

7038198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361515-G-T

7038247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361466-A-G

7038247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361466-A-T

7038314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361416-C-T

7038442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361309-A-G

7038458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361293-G-A

7039219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361186-A-G

7039246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361162-G-T

7039262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361146-A-G

7039324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361089-A-G

7039365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361047-T-G

7039486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26360926-G-T

7039516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26360899-T-C

7039516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26360899-T-G

7039526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26360889-G-A

7039617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26360796-T-C

7039701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, missense_variant
orthologous variants: 26360714-T-A

7039701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, missense_variant
orthologous variants: 26360714-T-C

7039740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, missense_variant
orthologous variants: 26360675-G-A

7039767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360647-C-G

7039767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360647-C-T

7039770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360644-G-A

7039770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360644-G-T

7039847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360576-T-A

http://identifiers.org/hco/2/GRCh38#7039867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26360556-C-A

http://identifiers.org/hco/2/GRCh38#7039913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26360513-C-A

7039913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360513-C-T

7039916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360510-T-C

7040064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26360339-T-C

7040426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359950-T-C

7040571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359824-T-A

7040571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359824-T-C

http://identifiers.org/hco/2/GRCh38#7040577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26359818-C-A

http://identifiers.org/hco/2/GRCh38#7040586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26359802-C-A

7040586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359802-C-T

http://identifiers.org/hco/2/GRCh38#7040616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26359772-C-A

7040616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359772-C-T

7040628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359760-T-C

7040716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359675-T-C

7040716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359675-T-G

7041014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359310-T-C

7041327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26359096-T-G

http://identifiers.org/hco/2/GRCh38#7041447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26358976-C-A

7041456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358967-C-G

7041650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358851-T-C

7041661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358840-G-A

7041671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358830-T-C

http://identifiers.org/hco/2/GRCh38#7041673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26358828-C-A

7041673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358828-C-T

7041683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358818-T-A

7041683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358818-T-C

7041709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358797-G-A

7041709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358797-G-T

7041817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358725-T-C

7041821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358721-A-G

7041840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358717-G-A

7041840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358717-G-T

http://identifiers.org/hco/2/GRCh38#7041854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26358703-C-A

7041854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358703-C-G

7041987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358585-G-A

7041989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358583-A-G

7042010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358572-A-G

7042010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358572-A-T

http://identifiers.org/hco/2/GRCh38#7042030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26358556-C-A

7042062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358527-G-T

7042116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358486-T-C

7042125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358477-C-G

7042165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358437-C-T

7042180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358420-C-T

7042197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358394-G-A

7042197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358394-G-T

http://identifiers.org/hco/2/GRCh38#7042235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26358356-C-A

7042243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358348-G-T

http://identifiers.org/hco/2/GRCh38#7042278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26358314-C-A

7042281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358311-G-T

7042286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358309-G-T

http://identifiers.org/hco/2/GRCh38#7042320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26358277-C-A

7042358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358246-T-C

7042370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26358234-A-G

7043151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357859-A-G

7043151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357859-A-T

7043157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357853-C-T

http://identifiers.org/hco/2/GRCh38#7043159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26357851-C-A

7043183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357828-G-A

7043183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357828-G-T

http://identifiers.org/hco/2/GRCh38#7043219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26357792-C-A

7043349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357661-C-G

http://identifiers.org/hco/2/GRCh38#7043456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26357552-A-C

7043456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357552-A-T

7043460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357548-C-G

7043460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357548-C-T

7043500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357504-A-G

http://identifiers.org/hco/2/GRCh38#7043694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26357311-C-A

7043694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357311-C-T

http://identifiers.org/hco/2/GRCh38#7043877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26357127-A-C

7043877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357127-A-G

7043890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357106-A-G

7043895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26357101-T-C

7044307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, undefined
orthologous variants: 26356712-T-A

7044307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, undefined
orthologous variants: 26356712-T-C

7044307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, undefined
orthologous variants: 26356712-T-G

7044413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26356000-A-G

7044476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, undefined
orthologous variants: 26355940-C-G

7044717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26355056-T-C

7044847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354939-G-C

7044957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354601-A-G

7045014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354507-A-G

7045019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354501-A-G

7045058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354466-A-G

7045142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354390-C-G

7045142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354390-C-T

7045183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron variant
orthologous variants: 26354349-G-A

7049487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353402-A-G

http://identifiers.org/hco/2/GRCh38#7050500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26352827-A-C

7057766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351942-A-G

7057766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351942-A-T

7057777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351907-T-G

7057983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351747-G-T

http://identifiers.org/hco/2/GRCh38#7060242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26350981-A-C

7060758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26350506-C-T

7060885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26350402-G-C

http://identifiers.org/hco/2/GRCh38#7061237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26350075-A-C

7061904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26349382-C-T

http://identifiers.org/hco/2/GRCh38#7063200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26347280-C-A

7063282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26347199-T-C

7063338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26347163-A-G

7063404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26347094-G-T

7063591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26346920-G-T

http://identifiers.org/hco/2/GRCh38#7063629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26346882-C-A

http://identifiers.org/hco/2/GRCh38#7063647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#26346864-A-C

7063694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26346827-T-G

7063729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26346792-G-T

7063761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26346764-C-G