112040840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: 59314811-T-C

http://identifiers.org/hco/9/GRCh38#112040985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59314930-A-C

112040986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: 59314931-C-G

http://identifiers.org/hco/9/GRCh38#112041005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59314949-C-A

112041005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: 59314949-C-G

112041005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: 59314949-C-T

http://identifiers.org/hco/9/GRCh38#112041057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59314995-A-C

112041073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3 prime UTR variant
orthologous variants: 59315011-T-C

http://identifiers.org/hco/9/GRCh38#112041150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59315084-C-A

112041150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 59315084-C-T

112041190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 59315135-C-T

112041249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 59315184-T-C

112041272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 59315209-G-A

112041386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 59315319-G-T

112041472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 59315397-C-T

112041731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 59315606-G-A

112041731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 59315606-G-C

112041731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 59315606-G-T

112041735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 59315610-G-A

112041735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 59315610-G-T

112041773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 59315628-C-G

112041773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 59315628-C-T

112041886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 59315731-G-A

112041946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 59315791-G-A

112041964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 59315809-T-C

http://identifiers.org/hco/9/GRCh38#112042009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59315854-C-A

112042014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59315886-A-G

112042106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59315980-T-A

http://identifiers.org/hco/9/GRCh38#112042185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59316057-C-A

112042185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59316057-C-T

112042188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59316060-G-A

112042220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59316088-T-A

112042296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59316160-T-C

112042333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59316194-C-G

112042520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59316376-A-G

112042818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59317026-T-C

112043678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

112044252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59317495-C-T

112044337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59317584-G-A

112044642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59317866-C-T

112044741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59317967-G-C

112044817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59318032-C-T

http://identifiers.org/hco/9/GRCh38#112044869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59318092-C-A

112044958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59318166-T-G

112044995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59318199-C-T

http://identifiers.org/hco/9/GRCh38#112045533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59318682-C-A

112045533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59318682-C-T

112045771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59318888-C-T

112045833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59318950-G-T

112045901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59318977-C-G

112045964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59319037-A-G

112046112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59319410-T-C

112046294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59319568-C-G

112046294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59319568-C-T

112048126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59320635-C-T

112048136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59320643-C-T

112048170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59320676-G-T

112048587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59321366-G-T

http://identifiers.org/hco/9/GRCh38#112048767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59321550-A-C

112049049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59321827-G-A

112049111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59321885-A-G

112049125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59321899-G-A

112049401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322126-C-T

112049452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322165-A-G

112049499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322209-T-C

112049500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322210-C-T

112049526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322230-T-C

112049657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322355-G-C

112049657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322355-G-T

112049862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59322518-C-T

http://identifiers.org/hco/9/GRCh38#112050137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59322767-A-C

112050457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59323046-C-T

112050924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59323473-C-T

112051006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59323535-A-G

http://identifiers.org/hco/9/GRCh38#112051026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59323562-A-C

112051757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59324272-G-A

112051804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59324319-T-C

112051894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59324402-T-A

112051894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59324402-T-C

http://identifiers.org/hco/9/GRCh38#112052217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59324668-C-A

112052217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59324668-C-T

112052337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59324801-T-C

112052381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59324850-G-A

112052498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325003-T-C

112052521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325026-G-T

112052541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325046-T-A

112052566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325073-G-A

112052566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325073-G-T

112052591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325116-G-A

112052722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325332-A-G

112052774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325384-T-G

112052818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59325420-G-C

112053073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59326232-G-T

112053198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59326371-T-G

112053958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59326772-A-G

112053982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59326796-T-G

112054015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59326829-G-A

112054015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59326829-G-T

112054253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59327007-A-G

112057637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59328652-T-C

112057801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59328780-C-T

112058048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59328905-T-G

112058184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59329029-A-T

112058244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59329084-A-G

http://identifiers.org/hco/9/GRCh38#112058382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59329417-C-A

112058382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59329417-C-T

112058397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59329432-A-G

112058397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59329432-A-T

112058414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59329449-G-C

112058462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59329497-C-T

http://identifiers.org/hco/9/GRCh38#112058533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59329568-C-A

http://identifiers.org/hco/9/GRCh38#112059287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59330010-C-A

112059287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330010-C-T

112059350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330071-G-A

112059350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330071-G-C

112059412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330135-G-A

112059412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330135-G-C

112059806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330501-C-T

112059906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330614-C-G

112059951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330803-G-A

112059951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330803-G-C

112059951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330803-G-T

http://identifiers.org/hco/9/GRCh38#112059962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59330814-C-A

112059963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330815-C-T

http://identifiers.org/hco/9/GRCh38#112059967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59330819-A-C

112059999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330880-C-T

112060000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330881-G-A

112060146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331027-T-C

112060172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331053-C-T

112060184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331065-G-A

112060708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331295-T-G

112060786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331356-C-G

112060786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331356-C-T

112060912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331427-G-A

112060912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331427-G-C

112061070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331547-T-A

112061149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331627-A-G

112061221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59331657-T-C

http://identifiers.org/hco/9/GRCh38#112061432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59331855-C-A

http://identifiers.org/hco/9/GRCh38#112061490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59331912-C-A

112061490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59331912-C-T

112061876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332310-C-T

112062178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332607-C-T

112062757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332785-G-A

112062791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332819-A-G

112062876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332900-A-G

112062897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332904-G-T

112063516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59333485-G-A

112063753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334090-G-A

112063935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334276-A-G

112063994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334329-A-G

112064012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334360-C-T

112064014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334362-C-T

http://identifiers.org/hco/9/GRCh38#112065611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59335017-C-A

112065778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335168-C-G

112066752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335841-C-G

112066945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335967-G-A

112067294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59336044-C-T

112067394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59336136-T-C

112070364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59337502-G-A

http://identifiers.org/hco/9/GRCh38#112070391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59337529-A-C

112070434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59337571-C-G

112070480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59337615-T-G

http://identifiers.org/hco/9/GRCh38#112070654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59337775-C-A

http://identifiers.org/hco/9/GRCh38#112071459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59338596-C-A

112071564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59338700-A-G

112072499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59338958-C-G

112072636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339162-T-G

112072808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339311-A-G

112072812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339315-G-C

112072895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339394-C-G

112072909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339410-G-T

112073062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339574-T-C

112073082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339594-C-T

112073103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339616-G-C

http://identifiers.org/hco/9/GRCh38#112073457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59339882-C-A

112073502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59339941-C-T

112074261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340052-T-C

112074476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340249-C-T

112074492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340265-T-C

112074492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340265-T-G

112074497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340270-A-G

112074709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59340481-C-T

112074789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59340549-G-A

112074790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59340550-G-T

http://identifiers.org/hco/9/GRCh38#112074901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59340888-C-A

112074954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59340940-G-C

http://identifiers.org/hco/9/GRCh38#112075026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59341035-C-A

112075041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341056-T-C

112075160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341178-G-A

112075160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341178-G-C

112075427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341417-T-G

http://identifiers.org/hco/9/GRCh38#112078398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59349699-C-A

112078398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59349699-C-T

112078479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59349777-G-A

112078479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59349777-G-C

112078479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59349777-G-T

112078505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59349793-T-C

http://identifiers.org/hco/9/GRCh38#112078791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59350065-C-A

112078791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350065-C-T

http://identifiers.org/hco/9/GRCh38#112078792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59350066-C-A

112078792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350066-C-G

112078792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350066-C-T

http://identifiers.org/hco/9/GRCh38#112078799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59350081-C-A

112078799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350081-C-T

112078810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350092-T-A

112078810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350092-T-C

112078810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350092-T-G

112078819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350110-T-C

112079241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350200-T-C

112080193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59351755-A-G

112080260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59351843-G-A

112080260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59351843-G-T

http://identifiers.org/hco/9/GRCh38#112080372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59351953-A-C

112080945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59352159-T-C

112081202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59352378-T-C

112081205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59352381-T-C

112081210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59352384-G-A

112081210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59352384-G-T

112081411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59352559-G-A

112084200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59358345-G-A

112084279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59358401-A-T

112084961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59358797-C-T

112085600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359739-A-T

112086285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360385-T-A

112086285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360385-T-C

112086285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360385-T-G

112086297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360396-A-G

112086520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360540-A-G

112086566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360595-G-A

112086581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360609-A-T

112086621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360646-G-A

112087786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59361534-G-A

112087897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59361647-C-T

112087982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59361743-G-A

112093074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363025-T-C

112093154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363115-C-G

112093314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363256-A-T

112093325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363267-G-C

112093739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363563-G-A

112093779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363593-G-A

112093824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363632-C-T

112093947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363759-A-T

112094142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363929-C-G

112097937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364375-G-A

112097948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59364386-G-C

112098166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365428-G-C

112098228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365489-G-A

112098229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365490-G-A

http://identifiers.org/hco/9/GRCh38#112098436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59365688-C-A

112098436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365688-C-T

112098579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59365831-A-G

112098579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59365831-A-T

112098685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365934-T-C

112098772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366001-T-C

112098772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366001-T-G

112098954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366166-G-A

112099513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366308-G-A

112099641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366432-G-T

http://identifiers.org/hco/9/GRCh38#112099724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59366507-C-A

112099903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366675-T-C

112100106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366877-C-G

112100142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59366913-T-C

112102152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59369506-G-A

112102152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59369506-G-T

http://identifiers.org/hco/9/GRCh38#112102230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59369585-A-C

112102252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59369607-T-C

112102318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59369670-T-C

http://identifiers.org/hco/9/GRCh38#112102785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59370912-C-A

112102785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370912-C-T

112103196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59371650-G-T

http://identifiers.org/hco/9/GRCh38#112103231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59371685-C-A

112103263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59371717-G-A

http://identifiers.org/hco/9/GRCh38#112103370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59371811-A-C

112103599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372033-T-A

112103599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372033-T-C

112103894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372316-C-G

112104002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372418-C-T

112104381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372576-A-G

112104450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372618-G-C

112104612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372791-A-G

112104631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372806-G-A

112104631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372806-G-T

112104652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372827-G-T

http://identifiers.org/hco/9/GRCh38#112104699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59372874-C-A

112104699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372874-C-T

112104704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372879-T-C

112104760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59372933-G-T

112104767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59372940-C-G

112105211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59373393-G-C

http://identifiers.org/hco/9/GRCh38#112105357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59373544-C-A

112105357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59373544-C-G

112105385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59373578-T-A

112110944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379250-T-C

112111504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379472-G-A

112111504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379472-G-T

112111515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379483-G-A

112111515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379483-G-C

112111515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379483-G-T

http://identifiers.org/hco/9/GRCh38#112111534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59379502-C-A

112111901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59379847-T-C

112112001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59379971-G-A

112112001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59379971-G-C

112112001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59379971-G-T

112112101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380049-G-A

112112101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380049-G-C

112112101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380049-G-T

112112137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380075-G-A

112112141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380079-C-G

112112141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380079-C-T

http://identifiers.org/hco/9/GRCh38#112112213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59380150-A-C

http://identifiers.org/hco/9/GRCh38#112112686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59380787-C-A

112112710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380809-A-T

112112715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380814-T-C

112112809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59380899-T-C

112112841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59380931-G-A

http://identifiers.org/hco/9/GRCh38#112112938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59381038-A-C

112112938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381038-A-G

112112990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59381090-A-T

http://identifiers.org/hco/9/GRCh38#112113188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59381272-C-A

112113206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59381290-G-A

112113222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59381306-A-G

112113462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381541-G-A

112113462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381541-G-T

112113639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381700-A-G

112114581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382027-T-C

112114612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382057-T-C

112114686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382112-T-C

112114846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382269-C-G

112115113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383222-G-A

112115187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383289-C-T

112115852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383598-T-A

112115852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383598-T-C

112115852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383598-T-G

112116050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383790-A-G

http://identifiers.org/hco/9/GRCh38#112116085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59383824-C-A

112116716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385682-A-G

112116718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385684-G-A

112116735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385700-C-T

112117205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385832-C-T

http://identifiers.org/hco/9/GRCh38#112117282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59385936-A-C

112117315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385968-G-T

112117450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386104-C-T

112117801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386412-T-C

112117850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386458-G-T

112118056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386636-C-G

112118076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386654-T-C

112118412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386945-G-A

112118412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386945-G-C

112119396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59387769-G-A

112119396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59387769-G-T

112119553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59387925-T-G

112119730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59388108-G-A

112119730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59388108-G-C

http://identifiers.org/hco/9/GRCh38#112119835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#59388211-C-A

112119889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59388265-C-T

112120424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388526-G-C

112120715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388806-C-T

112120757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388848-T-C

http://identifiers.org/hco/9/GRCh38#112124135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59390470-C-A

112124150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390485-G-A

112124150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390485-G-T

112124235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390548-G-A

112124512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390827-A-T

112124557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390870-T-A

112124557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390870-T-C

112124624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390968-G-C

112124687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391028-T-A

112124843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391183-A-G

112124871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391210-G-C

112125034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391379-T-C

112125632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59393526-A-G

112125636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59393530-G-A

112125636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59393530-G-T

112125762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59393655-C-T

112125874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59393994-G-A

112126213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59394486-T-C

112126310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59394614-G-T

112126428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394731-T-C

http://identifiers.org/hco/9/GRCh38#112126610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59394886-C-A

112131341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399267-G-A

112131341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399267-G-T

112131701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399980-G-A

112131929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400208-G-A

112132074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400323-T-C

112132163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400410-C-T

112132275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400523-A-T

http://identifiers.org/hco/9/GRCh38#112132357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59400607-C-A

112132359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400609-C-T

112132369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400619-T-A

112132370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400620-C-G

112132492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400735-A-G

112132677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400869-T-C

112132719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400894-T-C

112132807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401028-T-C

112135162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401263-C-T

112135225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401333-C-G

112135308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401413-T-G

112135512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401611-T-C

112141857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410864-G-A

112141857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410864-G-T

112141969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410953-C-T

112142190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411155-T-C

http://identifiers.org/hco/9/GRCh38#112142214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59411179-A-C

112142214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411179-A-T

112142313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59411263-A-G

112142552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59411502-A-T

http://identifiers.org/hco/9/GRCh38#112142568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59411518-C-A

http://identifiers.org/hco/9/GRCh38#112142628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59411561-C-A

http://identifiers.org/hco/9/GRCh38#112142685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59411617-C-A

112142685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411617-C-T

http://identifiers.org/hco/9/GRCh38#112142690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59411622-C-A

112143237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411937-C-T

112143255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411955-A-G

112143259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411959-T-C

112143301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412008-T-C

http://identifiers.org/hco/9/GRCh38#112143400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59412101-C-A

112143447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412147-C-T

112143573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59412272-C-T

112143653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412354-A-G

112143688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412373-G-A

112143688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412373-G-T

112143739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412423-T-C

http://identifiers.org/hco/9/GRCh38#112143741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59412425-C-A

112143741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412425-C-T

112143757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412441-T-C

112144624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413089-T-C

112144742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413211-C-T

112144808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413236-T-C

112144919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413269-T-C

112144979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413316-G-C

112145013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413349-G-A

112145130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413430-G-A

112145842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420480-G-A

112145908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420545-C-G

112145908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420545-C-T

112145909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420546-T-C

112145949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420582-C-T

http://identifiers.org/hco/9/GRCh38#112145974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59420593-C-A

112145974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420593-C-T

112146175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59420778-T-C

112146212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420823-G-A

http://identifiers.org/hco/9/GRCh38#112146240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59420845-C-A

112146240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420845-C-G

http://identifiers.org/hco/9/GRCh38#112146264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59420868-C-A

112146264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420868-C-G

112146264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420868-C-T

112146274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420878-A-G

112147672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59421785-A-G

112148044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59422100-G-A

112149200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423937-C-G

112149239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423990-A-G

112149302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59424053-T-A

112149408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424165-A-G

112149408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424165-A-T

112149413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424170-G-T

112149463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424219-C-G

112149463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424219-C-T

112149542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424282-T-C

http://identifiers.org/hco/9/GRCh38#112149890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59425463-A-C

112155373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426433-G-A

112155567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426712-C-G

112155656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426851-T-C

http://identifiers.org/hco/9/GRCh38#112155714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59426909-C-A

112155805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427015-T-A

112155899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427099-G-A

112155921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427121-G-A

112155926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427126-A-G

112156841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427438-T-C

112156900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427491-G-A

112156900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427491-G-C

112156909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427500-T-G

112157286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427735-G-A

http://identifiers.org/hco/9/GRCh38#112157417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59427870-C-A

112157417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427870-C-G

112157417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427870-C-T

http://identifiers.org/hco/9/GRCh38#112157422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59427876-A-C

112157422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427876-A-G

112157422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427876-A-T

112157488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427940-T-A

112157488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427940-T-C

112157489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427941-T-C

http://identifiers.org/hco/9/GRCh38#112157594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59428045-A-C

112157606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59428057-G-A

112157684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428127-A-G

112158729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428505-C-T

112158982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428937-G-T

112159195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59429134-T-C

112159263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59429200-C-T

112159319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59429256-A-G

112159714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59429693-A-T

112160053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59429786-G-C

112168226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59431904-C-G

112168433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59432126-G-A

http://identifiers.org/hco/9/GRCh38#112169439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59433343-A-C

112169441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433345-C-T

http://identifiers.org/hco/9/GRCh38#112169446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59433350-C-A

http://identifiers.org/hco/9/GRCh38#112169461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59433365-C-A

112169461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433365-C-T

112169512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433432-A-T

112169574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433535-A-G

112169650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433615-T-C

112173073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59435933-T-C

112173120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59435978-T-C

112174224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437345-A-G

112174228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437349-G-A

112174352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437472-T-C

112174697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437879-T-A

112174802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437974-G-A

112175043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59438164-A-G

112175043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59438164-A-T

112175138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59438211-G-A

112175138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59438211-G-T

http://identifiers.org/hco/9/GRCh38#112175141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59438214-C-A

112175141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59438214-C-G

112175141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59438214-C-T

112175170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59438243-G-A

112175170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59438243-G-T

112175183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59438256-A-G

http://identifiers.org/hco/9/GRCh38#112175224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59438312-C-A

112175224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59438312-C-G

112175224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59438312-C-T

http://identifiers.org/hco/9/GRCh38#112175231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59438319-C-A

112175231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59438319-C-G

112175231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59438319-C-T

http://identifiers.org/hco/9/GRCh38#112175254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#59438340-C-A

112175254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59438340-C-G

112175254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59438340-C-T

112175290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59438372-G-A

112175290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59438372-G-T