http://identifiers.org/hco/5/GRCh38#612343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#74210401-C-A

612343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74210401-C-G

612343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74210401-C-T

http://identifiers.org/hco/5/GRCh38#612450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#74210295-C-A

612450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 74210295-C-G

612450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 74210295-C-T

618548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74208128-G-A

618548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74208128-G-C

618716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207955-C-T

618717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207954-G-A

618743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207926-C-T

618839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207847-G-A

618839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207847-G-C

618839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207847-G-T

http://identifiers.org/hco/5/GRCh38#618917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74207760-A-C

618917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207760-A-T

618933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207744-T-G

618992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74207684-G-C

619211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207468-G-A

619211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207468-G-T

619224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74207455-T-A

619640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74206990-A-T

620171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74206509-G-A

622188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74205049-A-G

622944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74204342-A-G

http://identifiers.org/hco/5/GRCh38#624422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74203177-C-A

624422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74203177-C-G

624422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74203177-C-T

624601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74202981-A-G

624627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74202954-G-A

624627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74202954-G-C

624627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74202954-G-T

624628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74202953-C-T

624661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74202917-T-A

629388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74201356-A-G

http://identifiers.org/hco/5/GRCh38#633771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74201174-C-A

633771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74201174-C-G

633771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74201174-C-T

633949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 74200996-T-A

633949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 74200996-T-C

633955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74200990-G-C

633955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74200990-G-T

633985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200952-T-A

634119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200887-G-A

634119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200887-G-T

634402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200624-T-C

634427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200599-C-G

634427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200599-C-T

634433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200594-C-T

634434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200593-G-A

634434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200593-G-T

634548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200545-C-T

634562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200532-C-T

634564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74200530-C-T

635308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74199780-A-G

http://identifiers.org/hco/5/GRCh38#635380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74199730-C-A

635380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74199730-C-T

635433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74199677-G-C

635514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74199599-G-A

636492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74199151-T-C

636969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74199046-G-A

636969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74199046-G-C

637087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198939-T-C

637091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198935-C-T

637311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198705-C-T

http://identifiers.org/hco/5/GRCh38#637386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74198630-A-C

637386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198630-A-G

http://identifiers.org/hco/5/GRCh38#637408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74198609-C-A

637408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198609-C-G

637408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198609-C-T

637419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198589-T-C

637419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198589-T-G

http://identifiers.org/hco/5/GRCh38#637489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74198509-C-A

637489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74198509-C-T

638369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74197719-A-G

639191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74197046-T-C

http://identifiers.org/hco/5/GRCh38#639198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74197039-C-A

639238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74196999-G-A

640455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74195302-C-G

http://identifiers.org/hco/5/GRCh38#640610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74195147-C-A

640610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74195147-C-T

640683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74195041-T-C

http://identifiers.org/hco/5/GRCh38#640718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74195025-C-A

640718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74195025-C-T

http://identifiers.org/hco/5/GRCh38#640733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74195006-A-C

643376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74193070-G-A

643389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74193057-G-A

643481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192981-A-G

http://identifiers.org/hco/5/GRCh38#643581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74192909-C-A

643581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192909-C-T

http://identifiers.org/hco/5/GRCh38#643617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74192876-A-C

643617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192876-A-G

643660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192854-C-G

643668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192846-A-G

643677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192836-G-A

643677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192836-G-T

643712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74192811-G-A

644266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191778-T-G

644291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74191757-G-A

644407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74191641-T-G

646279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74189654-C-G

646397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74189501-C-T

646512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74189384-G-T

646645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74189267-G-A

647280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188694-G-A

647694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188374-T-A

647694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188374-T-G

http://identifiers.org/hco/5/GRCh38#647696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74188372-C-A

647696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188372-C-T

647733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188336-T-C

647733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188336-T-G

647815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74188269-A-G

647921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188163-C-G

647921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188163-C-T

648007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188116-A-T

648191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187939-C-T

648192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187938-A-G

648216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187912-A-G

651562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187727-T-C

651592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187701-G-C

651649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187647-A-T

651827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187528-C-T

651845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187510-T-C

651986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187405-G-A

651988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187403-C-G

651988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187403-C-T

http://identifiers.org/hco/5/GRCh38#652243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74187162-A-C

652283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187131-G-A

652322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74187091-G-A

652550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186919-A-G

652876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186570-G-T

652892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186547-G-A

652892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186547-G-T

652911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186525-G-A

652911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186525-G-C

652920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186515-A-G

http://identifiers.org/hco/5/GRCh38#652935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74186502-C-A

652935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186502-C-T

652995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74186438-G-A

652995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74186438-G-T

653007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74186426-G-A

653007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 74186426-G-T

653027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74186406-G-C

653069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74186364-G-A

http://identifiers.org/hco/5/GRCh38#653129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74186304-C-A

653129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74186304-C-T

http://identifiers.org/hco/5/GRCh38#653168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74186268-C-A

653168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74186268-C-T

653191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74186250-G-A

653191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74186250-G-T

http://identifiers.org/hco/5/GRCh38#653220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74186222-C-A

653220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74186222-C-T

653231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74186211-A-G

653231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74186211-A-T

653341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74186125-A-G

653341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74186125-A-T

653364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74186102-T-C

653395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74186081-A-G

http://identifiers.org/hco/5/GRCh38#653396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74186080-C-A

653414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74186072-T-C

653414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74186072-T-G

http://identifiers.org/hco/5/GRCh38#653499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74186014-A-C

653508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74186004-G-T

653624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74185883-T-C

653698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74185818-A-G

653698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74185818-A-T

658663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184759-T-A

658682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184740-T-G

658684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184738-T-C

658684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184738-T-G

http://identifiers.org/hco/5/GRCh38#658697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74184725-C-A

658697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184725-C-G

658697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184725-C-T

658959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184616-C-T

659596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184125-T-C

659644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184082-C-T

http://identifiers.org/hco/5/GRCh38#659825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74183909-C-A

660311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74183434-G-C

660311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74183434-G-T

660628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74183154-G-A

660628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74183154-G-C

660628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74183154-G-T

660654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74183108-C-T

660847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74182938-C-T

http://identifiers.org/hco/5/GRCh38#661134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74182661-C-A

661165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74182628-G-A

661240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74182502-T-C

661277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74182450-G-T

661434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74182251-A-G

661625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74182060-C-G

661625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74182060-C-T

661742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181949-G-A

661742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181949-G-T

http://identifiers.org/hco/5/GRCh38#661787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74181903-C-A

661787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181903-C-G

661787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181903-C-T

http://identifiers.org/hco/5/GRCh38#661916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74181790-C-A

661916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181790-C-T

661928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181778-T-C

http://identifiers.org/hco/5/GRCh38#662028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74181663-C-A

662028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181663-C-T

662077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181614-G-T

662158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181542-G-A

662158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181542-G-T

662201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181498-A-G

662270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181433-G-A

662270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181433-G-T

662277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181426-G-C

662277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181426-G-T

662472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181260-C-T

662577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181166-G-A

662577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181166-G-T

http://identifiers.org/hco/5/GRCh38#662597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74181146-C-A

662597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181146-C-T

662654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74181110-C-T

663516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74180916-G-A

663763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180686-A-G

663909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180548-T-C

http://identifiers.org/hco/5/GRCh38#663929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74180540-C-A

663929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180540-C-T

http://identifiers.org/hco/5/GRCh38#664021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74180500-C-A

664021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180500-C-T

http://identifiers.org/hco/5/GRCh38#664041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74180477-C-A

http://identifiers.org/hco/5/GRCh38#664104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74180403-C-A

664104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180403-C-T

664122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180391-G-C

664122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180391-G-T

664153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180371-G-A

664153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180371-G-T

664186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180340-G-A

664186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180340-G-T

http://identifiers.org/hco/5/GRCh38#664356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74180161-C-A

664404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74180115-G-A

http://identifiers.org/hco/5/GRCh38#664572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74179985-C-A

664572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179985-C-T

664587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179970-G-A

664587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179970-G-T

664695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179928-G-T

http://identifiers.org/hco/5/GRCh38#664711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74179910-C-A

664720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179901-T-C

664725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179896-G-A

664725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179896-G-T

http://identifiers.org/hco/5/GRCh38#664867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74179753-C-A

http://identifiers.org/hco/5/GRCh38#664885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74179734-C-A

664885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179734-C-T

664948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179670-G-A

664948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74179670-G-T

665238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74179396-G-T

http://identifiers.org/hco/5/GRCh38#665289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74179345-A-C

665965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25547
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74179025-C-T