http://identifiers.org/hco/11/GRCh38#74493869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99808340-C-A

74493890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99808318-G-C

74493890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99808318-G-T

74493935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99808284-G-A

74493935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99808284-G-C

74493935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99808284-G-T

http://identifiers.org/hco/11/GRCh38#74493942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99808277-C-A

74493942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99808277-C-T

74494020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99808137-G-C

74494020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99808137-G-T

74494047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99808110-T-A

74494047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99808110-T-G

74494155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99808007-G-A

74494155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99808007-G-T

74494377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99807803-C-T

74494389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99807791-C-G

74494421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99807777-A-T

74505838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99806677-T-A

http://identifiers.org/hco/11/GRCh38#74505866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99806650-A-C

74505866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99806650-A-G

http://identifiers.org/hco/11/GRCh38#74506074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99806479-C-A

74506301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99806255-A-G

74506306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99806250-A-G

74506393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99804229-C-T

74506803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99803708-A-G

74506825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99803686-G-A

74508289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99800827-C-T

74521049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99800153-G-A

74521374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99799799-C-T

74521377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99799796-C-T

74521533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99799640-C-T

74522000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99799229-C-T

74522240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99798511-A-G

74522287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99798475-G-A

74522292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99798470-G-A

74522371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99798392-C-G

74522517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99798249-T-G

74522763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99798041-A-G

74524565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99797436-C-T

74524613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99797390-C-G

http://identifiers.org/hco/11/GRCh38#74524644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99797369-C-A

74524847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99797188-T-C

http://identifiers.org/hco/11/GRCh38#74524861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99797175-C-A

74524884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99797152-G-A

http://identifiers.org/hco/11/GRCh38#74559856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99786462-C-A

74559883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, undefined
orthologous variants: 99786435-T-C

74559934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, undefined
orthologous variants: 99786384-C-T

74560004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99786313-T-C

74564949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99784861-G-C

74565283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99783121-T-C

74565286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99783118-C-G

74576738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99777671-G-A

74576910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99777510-G-A

74576910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99777510-G-C

74579385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99776739-T-C

74579473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99776644-G-C

74579757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99776097-A-T

http://identifiers.org/hco/11/GRCh38#74579853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99775999-C-A

74579853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99775999-C-T

74582371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, undefined
orthologous variants: 99773809-C-T

74583234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99773316-G-A

74583917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99773115-C-T

74584037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99773007-T-C

74584098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99772960-T-C

74584131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99772926-C-T

http://identifiers.org/hco/11/GRCh38#74585282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99772426-A-C

74585602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99772135-C-T

http://identifiers.org/hco/11/GRCh38#74586381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99771492-A-C

http://identifiers.org/hco/11/GRCh38#74592481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770797-C-A

74592481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, undefined
orthologous variants: 99770797-C-T

74592580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770699-G-A

http://identifiers.org/hco/11/GRCh38#74592606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770673-C-A

74592606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770673-C-T

74592607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770672-T-C

74592628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770659-G-A

74592628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770659-G-C

74592628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770659-G-T

74592632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770655-A-G

74592632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99770655-A-T

74592740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770539-A-G

74592791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770477-G-C

74592791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770477-G-T

http://identifiers.org/hco/11/GRCh38#74592794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770474-C-A

74592794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770474-C-T

74592887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99770396-C-G

74592887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99770396-C-T

http://identifiers.org/hco/11/GRCh38#74592919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770365-C-A

74592919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770365-C-G

74592919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770365-C-T

74592923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770361-G-T

http://identifiers.org/hco/11/GRCh38#74592941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770343-C-A

74592941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770343-C-T

74592942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770342-T-C

74592942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770342-T-G

74592961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770328-T-C

http://identifiers.org/hco/11/GRCh38#74592975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770314-C-A

74592975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770314-C-T

74593043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770269-T-C

74593047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770265-G-A

74593047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770265-G-T

74593051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770261-A-G

http://identifiers.org/hco/11/GRCh38#74593052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770260-A-C

74593090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99770239-T-A

74593091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99770238-G-C

74593092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99770237-T-A

74593092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99770237-T-C

http://identifiers.org/hco/11/GRCh38#74593114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99770211-C-A

74593114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99770211-C-T

74593286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99770067-C-G

74593286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99770067-C-T

74593580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99769779-T-G

74593589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99769773-T-C

74593652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99769696-G-C

74593929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99769064-T-C

74594030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99768963-A-G

74594130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99768865-A-G

74594130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99768865-A-T

http://identifiers.org/hco/11/GRCh38#74601295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99763574-A-C

74601363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99763507-G-A

74601390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99763481-C-T

http://identifiers.org/hco/11/GRCh38#74601509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99763364-A-C

74601509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99763364-A-G

74601510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99763363-G-A

http://identifiers.org/hco/11/GRCh38#74603500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99762763-C-A

74603738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99762580-G-A

74603831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99762384-A-G

74603831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99762384-A-T

http://identifiers.org/hco/11/GRCh38#74604070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99762169-A-C

74604185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99762055-A-G

http://identifiers.org/hco/11/GRCh38#74604192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99762043-A-C

http://identifiers.org/hco/11/GRCh38#74604473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99761782-C-A

74604473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99761782-C-T

74604640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99761622-A-G

74604646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99761618-A-G

74604685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99761584-G-A

74604685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99761584-G-T

74604687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99761582-A-G

74604687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99761582-A-T

http://identifiers.org/hco/11/GRCh38#74604887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99761396-C-A

74604887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99761396-C-T

74605321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99760995-C-G

74611212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99757986-C-T

74611301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99757912-A-G

74611479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99757775-A-G

74611479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99757775-A-T

74611573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99757675-T-A

74611573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99757675-T-C

74611642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99757627-A-T

74611649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99757620-T-G

74612612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99756157-A-G

74612754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99756024-G-A

74612754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99756024-G-T

http://identifiers.org/hco/11/GRCh38#74612756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99756022-C-A

74612756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99756022-C-T

74612790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99755988-T-C

74612873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99755905-T-G

74613317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99755463-A-G

74613524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99755260-T-G

74614887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99754439-A-G

74615069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99754295-G-A

74615453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99753912-G-A

74615491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99753876-G-C

74615795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99753361-G-A

74616146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99753005-C-T

74616333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99751418-C-G

74616489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99751285-C-T

74617037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99750847-C-G

http://identifiers.org/hco/11/GRCh38#74617251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99750633-C-A

74617251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99750633-C-T

74617270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99750614-A-G

74617308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99750578-G-A

http://identifiers.org/hco/11/GRCh38#74618094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99750416-C-A

74618114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99750392-T-G

74618375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99750003-T-C

74618406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749962-G-A

74618419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749949-G-A

74618419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749949-G-T

74618865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749565-T-A

http://identifiers.org/hco/11/GRCh38#74619153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99749163-C-A

74619153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749163-C-G

74619170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749148-G-A

http://identifiers.org/hco/11/GRCh38#74619188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99749130-C-A

74619191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749127-A-G

74619191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99749127-A-T

74619501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99748782-A-G

74620127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99748631-A-G

http://identifiers.org/hco/11/GRCh38#74620164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99748598-C-A

74620164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99748598-C-G

74620164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99748598-C-T

74620191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99748572-A-G

74620471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99748307-T-G

74624386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99747073-A-G

74624610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99746847-A-G

74624622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99746836-G-A

74625160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745970-T-C

74625307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745832-T-C

74625594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745555-A-T

74625603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745540-G-A

74625615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745528-G-T

74625616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745527-G-A

74625653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745491-A-G

74625676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745468-C-G

http://identifiers.org/hco/11/GRCh38#74625679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99745465-C-A

http://identifiers.org/hco/11/GRCh38#74625700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99745444-C-A

74625722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745423-G-A

74625722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745423-G-T

74625776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99745371-G-A

74626308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99744862-C-T

74626639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99744541-A-G

74626715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99744447-G-C

74627976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99744158-A-G

http://identifiers.org/hco/11/GRCh38#74628659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99743519-C-A

74628659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99743519-C-T

74628780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99743411-C-T

74629019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99743115-A-G

74629021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99743113-G-A

74629021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99743113-G-T

74629201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99742698-T-C

74629309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99742591-G-A

74629309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99742591-G-T

http://identifiers.org/hco/11/GRCh38#74629454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99742467-C-A

74629454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99742467-C-G

74629454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99742467-C-T

74631229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741894-G-A

74631394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741756-C-T

http://identifiers.org/hco/11/GRCh38#74631960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99741651-C-A

74631960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741651-C-T

http://identifiers.org/hco/11/GRCh38#74631987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99741621-A-C

74632036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741583-C-T

74632087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741540-A-G

74632387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741243-T-A

74632423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741211-G-A

74632458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741176-C-T

74632467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99741164-G-A

74632630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99740915-A-G

74632836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99740738-A-G

74633052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99740588-G-A

74633664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99739894-T-C

74634365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99739322-C-T

74634529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99739011-T-C

http://identifiers.org/hco/11/GRCh38#74634562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99738981-A-C

74634562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99738981-A-G

http://identifiers.org/hco/11/GRCh38#74634675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99738871-C-A

74634675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99738871-C-T

http://identifiers.org/hco/11/GRCh38#74634793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99738757-C-A

74634793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99738757-C-T

74634796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99738754-A-G

74635250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99738344-C-T

74635886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99737592-C-G

74636189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99737355-C-G

74636329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99737246-A-G

http://identifiers.org/hco/11/GRCh38#74636390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99737189-C-A

74636390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99737189-C-G

74636390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99737189-C-T

74636399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99737181-T-C

74636420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99737160-G-A

74636420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99737160-G-T

74636664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99736947-G-A

74637251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99736310-T-C

74637380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99736194-C-T

74637513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99736088-A-G

74637853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99735809-A-T

74637865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99735797-G-T

http://identifiers.org/hco/11/GRCh38#74637928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99735736-A-C

74637934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99735730-C-T

74638941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99734764-A-G

74638966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99734741-T-G

74639468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99734163-G-T

http://identifiers.org/hco/11/GRCh38#74639528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99734108-A-C

74639632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99734040-G-A

74639708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99733961-G-A

74639708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99733961-G-T

74639862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99733621-G-A

74640213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99733320-A-T

74640295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99733242-G-A

74640431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99733127-A-G

74640578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99733045-T-C

74640740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99732883-A-G

74640778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732846-T-C

74640853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732776-T-G

http://identifiers.org/hco/11/GRCh38#74640894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99732736-C-A

74640894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732736-C-T

http://identifiers.org/hco/11/GRCh38#74641207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99732480-A-C

74641207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732480-A-G

http://identifiers.org/hco/11/GRCh38#74641208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99732479-C-A

74641216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732465-G-A

74641355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732330-C-T

74641476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732244-T-C

74641482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732238-C-G

74641482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732238-C-T

74641502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99732218-T-C

http://identifiers.org/hco/11/GRCh38#74641503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99732217-C-A

74641503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99732217-C-G

74641503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99732217-C-T

http://identifiers.org/hco/11/GRCh38#74641517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99732204-C-A

74641517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99732204-C-T

74641532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732189-T-C

74641536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732185-G-A

74641541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732180-G-A

74641541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732180-G-T

74641543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732178-T-C

74641554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732167-G-A

74641554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732167-G-T

74641624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99732101-C-T

74641663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732063-C-T

74641695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732046-T-C

74641715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99732027-A-G

74641814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731930-T-G

http://identifiers.org/hco/11/GRCh38#74641830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99731914-C-A

74641844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731900-A-G

74641950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731867-T-C

http://identifiers.org/hco/11/GRCh38#74641970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99731847-C-A

74641970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731847-C-G

74641970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731847-C-T

74641982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731835-T-C

74642037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731783-G-A

74642133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731698-G-A

74642133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731698-G-T

74642395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731450-C-T

http://identifiers.org/hco/11/GRCh38#74642418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99731427-C-A

74642419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731426-A-G

74642439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731406-T-C

74642526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731322-A-G

74642593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731260-A-G

74642767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99731081-G-T

http://identifiers.org/hco/11/GRCh38#74642785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99731063-A-C

http://identifiers.org/hco/11/GRCh38#74643079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99730783-C-A

74643079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99730783-C-G

74643102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99730756-G-A

74643102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99730756-G-T

74643157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99730715-T-A

74643591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99730287-A-G

74643629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99730253-G-A

74643693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99730017-T-C

74643930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99729738-A-G

74644865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99728841-C-T

74644942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99728758-G-A

74645422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99728380-G-A

74645589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99728240-C-T

74645590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99728239-T-C

http://identifiers.org/hco/11/GRCh38#74645920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99727726-A-C

74646300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99727479-C-T

74646635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99727150-C-T

74646648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99727138-G-C

74648183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99725975-T-C

74648226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99725926-G-T

74648316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99725862-T-C

74648575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99725683-G-C

74648623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99725647-G-A

74649102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99725218-G-A

http://identifiers.org/hco/11/GRCh38#74649533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99724938-A-C

74649574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99724891-C-T

74649683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99724791-T-C

74650387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99723767-G-T

74650883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99723281-G-T

74651036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: intron variant
orthologous variants: 99723108-G-C

74669045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706945-G-T

74669081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706925-A-G

74669110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706896-G-A

74669110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706896-G-T

74669126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706880-C-G

74669126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706880-C-T

74669179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706827-A-G

74669179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: 99706827-A-T

http://identifiers.org/hco/11/GRCh38#74669316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20932
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99706705-C-A