64265352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121530934-G-T

64265392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121530880-G-A

64265392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121530880-G-T

64265438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121530848-A-G

64265470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121530816-A-G

64265869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529346-T-C

64265970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529285-G-T

64265990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529265-A-G

64266063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529206-G-A

64266118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529148-T-A

64266118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529148-T-C

64266126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529140-G-T

64266129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529131-G-T

http://identifiers.org/hco/12/GRCh38#64266182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121529073-C-A

64266226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121529030-T-C

64266271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121528999-G-A

64266271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121528999-G-T

64266300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121528968-G-A

64266300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121528968-G-C

64266300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121528968-G-T

64266322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121528940-T-C

64267042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121528493-G-T

64267139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121528414-T-C

64267374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121528151-G-A

64267374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121528151-G-T

64267526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527955-G-T

64267625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121527866-T-C

64267628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121527863-T-A

64267628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121527863-T-C

64267628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121527863-T-G

http://identifiers.org/hco/12/GRCh38#64267655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121527837-A-C

http://identifiers.org/hco/12/GRCh38#64267694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121527825-C-A

64267694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527825-C-T

http://identifiers.org/hco/12/GRCh38#64267707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121527812-C-A

64267707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527812-C-T

http://identifiers.org/hco/12/GRCh38#64267728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121527802-C-A

64267785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527761-C-G

64267785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527761-C-T

64268143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527657-A-G

64268152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527648-G-A

64268238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121527558-A-G

http://identifiers.org/hco/12/GRCh38#64268697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121526983-A-C

64269262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121526710-G-A

64269312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121526662-T-C

64269519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121526443-A-G

64269519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121526443-A-T

64269568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121526385-A-T

http://identifiers.org/hco/12/GRCh38#64270789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121525598-C-A

http://identifiers.org/hco/12/GRCh38#64270834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121525549-C-A

64270839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121525544-T-G

64270840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121525543-T-A

64270840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121525543-T-C

http://identifiers.org/hco/12/GRCh38#64270861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121525522-A-C

64270861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121525522-A-G

64270861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121525522-A-T

64270864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121525519-T-C

64271843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121524963-T-C

64271955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121524829-T-G

64272788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121524362-T-C

http://identifiers.org/hco/12/GRCh38#64272971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121524194-C-A

64273563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121523700-T-G

64273925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121523424-G-T

64274002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121523358-C-T

64274084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121523278-G-A

http://identifiers.org/hco/12/GRCh38#64274121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#121523239-C-A

64274121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121523239-C-T

64274447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121522256-C-G

http://identifiers.org/hco/12/GRCh38#64274844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121521839-A-C

64274844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121521839-A-G

64274844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121521839-A-T

64274944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121521755-G-A

64275024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521679-G-A

64275038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521665-A-G

64275040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521663-T-G

64275149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521602-G-A

64275149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521602-G-T

64275164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521587-T-C

64275164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521587-T-G

http://identifiers.org/hco/12/GRCh38#64275187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121521568-A-C

64275187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521568-A-G

64275239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521547-T-A

64275239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521547-T-C

64275239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521547-T-G

64275278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521525-A-G

64275307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121521506-G-A

64275307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121521506-G-T

64275316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121521497-T-A

64275316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521497-T-C

64275345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121521468-T-A

64275345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121521468-T-C

64275366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121521447-T-C

64275395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121521420-A-G

64275395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121521420-A-T

http://identifiers.org/hco/12/GRCh38#64275410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121521405-C-A

64275996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121520942-T-G

http://identifiers.org/hco/12/GRCh38#64277562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121520038-C-A

64277562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121520038-C-G

64277571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121520029-G-T

http://identifiers.org/hco/12/GRCh38#64277586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121520014-C-A

64277600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121520000-G-A

64277600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121520000-G-T

http://identifiers.org/hco/12/GRCh38#64277608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121519992-C-A

64277620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121519976-A-G

http://identifiers.org/hco/12/GRCh38#64277729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121519873-A-C

64277729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121519873-A-T

64277848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121519757-G-A

64277848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121519757-G-T

64277858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121519747-G-A

64277858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121519747-G-T

64279916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121516525-A-T

64280096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121516382-G-A

64280189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121516293-C-T

http://identifiers.org/hco/12/GRCh38#64280733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121515802-C-A

64280733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121515802-C-G

64280899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121515687-C-T

64280915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121515672-T-C

64281732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121515527-T-C

64281742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121515518-T-C

64281782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121515468-G-A

64281785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121515465-G-A

64284730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121514270-G-A

http://identifiers.org/hco/12/GRCh38#64284776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121514224-C-A

64284776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121514224-C-T

64284826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121514154-A-G

64284869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121514111-T-A

64284895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121514089-A-G

http://identifiers.org/hco/12/GRCh38#64285889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121513507-C-A

64285889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513507-C-T

64285937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513276-A-G

64285937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513276-A-T

64285952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 121513261-A-G

64285952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 121513261-A-T

http://identifiers.org/hco/12/GRCh38#64285969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121513244-C-A

64285969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121513244-C-G

64286068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121513145-A-G

64286073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121513140-G-A

64286073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121513140-G-C

64286073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121513140-G-T

64286103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513121-T-C

64286104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513120-G-A

64286104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513120-G-T

64286209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513023-A-G

64286209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513023-A-T

http://identifiers.org/hco/12/GRCh38#64286210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121513022-A-C

64286210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121513022-A-G

64286599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121512338-C-T

http://identifiers.org/hco/12/GRCh38#64299549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121510543-C-A

64299836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121510140-A-G

64300033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121509969-T-C

64300088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121509917-A-G

64302351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121509580-C-G

64302519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121509452-A-G

64302756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121509306-A-G

64302830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121509232-T-A

64303747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121507644-A-G

64303774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121507617-T-C

64303831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121507566-G-A

64303831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121507566-G-C

64303831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121507566-G-T

http://identifiers.org/hco/12/GRCh38#64303844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121507554-A-C

64303844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121507554-A-G

http://identifiers.org/hco/12/GRCh38#64303921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121507281-C-A

64303921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121507281-C-T

64304019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121507195-A-G

64304057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121507162-C-T

http://identifiers.org/hco/12/GRCh38#64304142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121507056-A-C

64312694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121505118-C-T

64312703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121505109-G-T

64312779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505030-T-C

64312799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121505011-G-A

64312896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121504915-A-G

http://identifiers.org/hco/12/GRCh38#64318449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121503849-C-A

64318470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503827-G-T

64318471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503826-G-T

64318476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503821-A-T

http://identifiers.org/hco/12/GRCh38#64318490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121503807-A-C

64318509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503791-G-A

64318509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503791-G-T

64318670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121503614-A-T

64318792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 121503489-T-A

64318890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 121503397-G-T

64318952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 121503338-T-C

64319007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121503284-A-G

64319011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121503280-C-T

64319028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503263-T-A

64319028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503263-T-G

64319051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121503226-T-A

64322719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499724-G-A

64322825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499612-G-A

64322864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499573-G-C

64322958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499485-C-T

64322991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499452-T-C

64323039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499401-A-G

64323103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499342-A-G

64330354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498424-T-C

64330375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498403-G-C

http://identifiers.org/hco/12/GRCh38#64330834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121497352-C-A

64330835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497351-A-G

64330890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497298-G-T

http://identifiers.org/hco/12/GRCh38#64331014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121496995-C-A

64331014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121496995-C-T

64331046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496962-T-A

64331046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496962-T-C

64331048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496960-G-A

64331048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496960-G-C

64331048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496960-G-T

64331051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496957-A-G

64331052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496956-T-A

64331052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496956-T-C

http://identifiers.org/hco/12/GRCh38#64333815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121496719-A-C

64334090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496498-A-G

64334209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495039-G-A

64334209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495039-G-T

http://identifiers.org/hco/12/GRCh38#64334232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121495019-A-C

64334262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494989-G-C

64334301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121494946-C-T

64335690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492936-A-G

64336050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492603-T-C

64336156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492500-A-G

64336209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492445-T-C

http://identifiers.org/hco/12/GRCh38#64336484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121492078-A-C

64336484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121492078-A-T

64336620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491945-T-G

64336803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491763-G-A

64352900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121490805-T-G

64352961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121490747-A-G

64352977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121490731-A-G

64352983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121490725-G-A

64352990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121490718-A-G

64353060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121490648-G-A

64353060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121490648-G-C

64353064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121490644-A-G

64353064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121490644-A-T

64373641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121489446-C-G

64373870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121489310-A-G

64374184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121489014-G-A

64374570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487843-G-A

64384607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121484778-G-A

64385001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121484284-C-T

64385031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121484248-G-A

http://identifiers.org/hco/12/GRCh38#64385032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121484247-C-A

http://identifiers.org/hco/12/GRCh38#64385287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121483987-C-A

64387209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121480561-T-G

64387250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121480521-C-T

64387336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121480474-C-T

64387921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479330-T-C

64387966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479286-C-T

64387967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121479285-G-A

http://identifiers.org/hco/12/GRCh38#64389151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121478668-C-A

64389151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121478668-C-T

64389219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121478596-G-A

http://identifiers.org/hco/12/GRCh38#64389229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121478586-C-A

64389229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121478586-C-T

64389417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478428-G-T

64390042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478204-G-A

64390212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478058-A-G

64390212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478058-A-T

http://identifiers.org/hco/12/GRCh38#64390235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121478025-C-A

64390251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478011-G-T

64390252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478010-G-A

64390252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478010-G-C

64390252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121478010-G-T

http://identifiers.org/hco/12/GRCh38#64390263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121477999-C-A

64390263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477999-C-T

64390303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477983-G-A

64390303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477983-G-C

64390303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121477983-G-T

64390435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121477851-T-A

64390435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121477851-T-C

64390435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121477851-T-G

64390489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121477797-G-T

64390520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121477766-G-A

64390520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121477766-G-C

64390520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 121477766-G-T

http://identifiers.org/hco/12/GRCh38#64390578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#121477710-C-A

64390578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477710-C-T

64390686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477616-G-T

64390692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477606-G-A

64390692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477606-G-T

64390717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477576-T-A

64390730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477563-G-A

64390730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477563-G-C