http://identifiers.org/hco/10/GRCh38#69220344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#62258219-C-A

69220411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62258161-T-C

69220416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62258156-A-G

http://identifiers.org/hco/10/GRCh38#69220421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62258151-C-A

69220421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62258151-C-T

69220555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62258020-G-A

69220555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62258020-G-T

69220622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62257860-G-A

69220622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62257860-G-T

69220817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62257691-A-G

69221398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62257179-G-A

69221398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62257179-G-C

69221398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62257179-G-T

69222495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62256711-C-T

69222744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62256515-T-C

69222760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62256505-G-A

69222760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62256505-G-T

http://identifiers.org/hco/10/GRCh38#69222762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#62256503-C-A

69222774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62256491-G-T

69222885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 62256390-A-G

http://identifiers.org/hco/10/GRCh38#69223082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#62256222-A-C

http://identifiers.org/hco/10/GRCh38#69223193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62256112-C-A

69223341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255878-A-G

69223367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255850-T-C

69223445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255798-T-C

69224713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255429-G-A

69224713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255429-G-C

69224713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255429-G-T

69224784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255354-T-C

69224833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255328-C-T

69224865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255298-G-A

69224892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255279-T-G

69224926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255254-A-G

69225008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255170-T-C

69225048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62255133-T-A

http://identifiers.org/hco/10/GRCh38#69225123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62255057-C-A

69225238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62254966-A-T

http://identifiers.org/hco/10/GRCh38#69227062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#62253858-C-A

69227107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62253824-A-T

69227147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62253784-G-A

69227173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62253753-A-G

69227191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62253730-C-T

69227202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62253719-T-C

69227360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62253561-G-A

http://identifiers.org/hco/10/GRCh38#69227508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62253436-C-A

69227632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62253326-C-T

69227734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62253227-C-T

69228375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62252300-C-T

69229125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62252014-G-T

69229232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62251932-T-A

69229232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62251932-T-C

69229232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62251932-T-G

69229330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62251879-G-T

69229406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62251808-G-A

69230094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62251199-G-C

69230231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62251081-G-A

http://identifiers.org/hco/10/GRCh38#69230404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62250843-C-A

69230454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62250793-C-T

69230505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62250741-C-G

69230505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62250741-C-T

69230977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62249695-G-T

69231115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62249532-C-T

69231116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62249531-G-A

69232332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62248075-G-A

69232332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62248075-G-T

69232340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62248067-C-T

http://identifiers.org/hco/10/GRCh38#69232353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62248046-C-A

69232353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62248046-C-G

69232355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62248044-G-A

69232355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62248044-G-T

http://identifiers.org/hco/10/GRCh38#69232370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62248029-C-A

69232370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 62248029-C-G

69232370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 62248029-C-T

69232528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62247850-G-A

69232641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247749-A-G

http://identifiers.org/hco/10/GRCh38#69232690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62247692-C-A

69232690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247692-C-T

69232943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247468-G-C

69232985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247428-C-G

69232993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247421-T-G

69233178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247258-G-A

69233181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247255-T-C

69233284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247188-G-A

69233284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62247188-G-T

69237815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62246869-G-C

69237955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62246760-T-A

69238927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245765-T-C

http://identifiers.org/hco/10/GRCh38#69238948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62245745-C-A

69238948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245745-C-G

69238948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245745-C-T

69238977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245714-T-C

69238980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245711-G-A

69238980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245711-G-T

69238983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245708-G-A

69238983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245708-G-T

http://identifiers.org/hco/10/GRCh38#69238986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62245705-C-A

69238986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62245705-C-T

http://identifiers.org/hco/10/GRCh38#69239180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62245533-C-A

69239180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245533-C-T

69239220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245512-G-A

69239220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245512-G-T

69239221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245511-G-A

http://identifiers.org/hco/10/GRCh38#69239270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62245479-C-A

69239270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245479-C-T

69239274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245475-G-A

69239274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245475-G-T

69239387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245396-C-T

69239409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62245370-C-T

69239647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

69240070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244788-C-T

69240080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244778-A-G

69240545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244571-A-T

69240658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62244485-G-T

69240691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62244452-G-A

69240691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62244452-G-T

69240762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244382-T-C

69240805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244351-G-A

http://identifiers.org/hco/10/GRCh38#69240821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62244335-C-A

69240874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244287-G-T

http://identifiers.org/hco/10/GRCh38#69240893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62244266-C-A

69240893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244266-C-T

69240895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62244263-T-C

69242176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242647-C-G

69242241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242578-T-A

69242241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242578-T-C

69242284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242519-T-C

69242295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242509-C-T

69242378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242414-T-A

69242378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242414-T-C

69242404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242388-G-C

69242404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242388-G-T

69242558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242229-G-A

69242693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62242108-A-T

69243013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62241581-C-G

69243067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62241525-G-A

69243067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62241525-G-C

69243067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62241525-G-T

http://identifiers.org/hco/10/GRCh38#69243101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62241495-A-C

69243101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62241495-A-G

69243280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62241287-T-C

http://identifiers.org/hco/10/GRCh38#69243352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62241215-C-A

69243352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62241215-C-G

69244900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62240524-G-C

69244900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62240524-G-T

69245219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62240234-T-C

69245272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62240183-T-G

69245888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62239513-G-A

http://identifiers.org/hco/10/GRCh38#69246073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62239430-C-A

69246073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62239430-C-T

http://identifiers.org/hco/10/GRCh38#69246194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62239309-A-C

69246194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62239309-A-G

69246249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62239122-C-T

69246268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62239103-G-A

http://identifiers.org/hco/10/GRCh38#69246275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62239096-A-C

69246275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62239096-A-T

http://identifiers.org/hco/10/GRCh38#69246365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62238975-C-A

69246365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62238975-C-G

69246365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62238975-C-T

69246403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62238937-A-G

http://identifiers.org/hco/10/GRCh38#69246499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62238834-C-A

69246980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62238436-G-A

69246989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62238427-C-T

69247018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62238397-G-A

69247107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237939-G-A

69247153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237891-G-T

69247175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237870-T-C

http://identifiers.org/hco/10/GRCh38#69247241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62237812-C-A

69247241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237812-C-G

69247241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237812-C-T

http://identifiers.org/hco/10/GRCh38#69247246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62237807-C-A

69247328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237765-G-A

http://identifiers.org/hco/10/GRCh38#69247338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62237755-C-A

http://identifiers.org/hco/10/GRCh38#69247614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62237481-A-C

69247614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237481-A-G

http://identifiers.org/hco/10/GRCh38#69247623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62237472-C-A

69247623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237472-C-T

69247624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237471-A-G

69247630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237465-G-A

69247648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237446-C-T

http://identifiers.org/hco/10/GRCh38#69247669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62237423-C-A

69247669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237423-C-G

69247669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62237423-C-T

69247834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236786-C-T

69247908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236718-A-T

69248248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236416-C-T

69248273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236401-T-A

69248273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236401-T-C

69248329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236375-G-A

69248329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236375-G-T

69248340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236364-G-A

69248340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236364-G-T

http://identifiers.org/hco/10/GRCh38#69248342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62236362-C-A

69248342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236362-C-T

http://identifiers.org/hco/10/GRCh38#69248358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62236347-C-A

69248358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236347-C-G

69248358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236347-C-T

69248364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236341-G-A

69248364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62236341-G-T

69248515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62236182-G-A

69248608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62236089-C-T

http://identifiers.org/hco/10/GRCh38#69248738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62235954-C-A

69249806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62235089-C-G

69250121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234839-T-A

69250236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234771-T-C

http://identifiers.org/hco/10/GRCh38#69250241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62234767-C-A

69250241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234767-C-G

69250241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234767-C-T

69250255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234753-G-A

http://identifiers.org/hco/10/GRCh38#69250257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62234739-C-A

69250455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234554-T-G

69250459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234550-G-A

69250459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234550-G-T

69250464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234545-C-G

69250464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234545-C-T

69250517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234493-C-G

69250517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234493-C-T

69250546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62234468-T-A

69250546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62234468-T-G

69250712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62234302-C-T

69256811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231447-G-A

69256834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231424-A-G

69256873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231409-T-C

69257155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231151-T-A

69257155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231151-T-C

69257175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231132-C-T

69257209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231103-T-C

69257209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62231103-T-G

69257363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62230995-A-G

http://identifiers.org/hco/10/GRCh38#69257453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62230910-C-A

69257508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62230872-A-G

69257559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62230814-G-T

69257564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62230809-T-A

69257564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62230809-T-C

69257564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62230809-T-G

69257807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62230619-G-T

69258471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62229925-G-A

69258614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62229807-G-A

69258706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62229717-T-C

http://identifiers.org/hco/10/GRCh38#69258817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62229606-A-C

69258817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62229606-A-T

69258829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62229594-G-A

69258868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62229555-G-A

69258868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 62229555-G-T

69265246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221984-A-G

69265260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221970-G-A

69265260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221970-G-C

69265303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221932-G-A

69265303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221932-G-T

69265304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221931-G-A

69265304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221931-G-C

69265310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221925-G-A

69265310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221925-G-T

69265339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221898-A-G

69265339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62221898-A-T

http://identifiers.org/hco/10/GRCh38#69265471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62221790-C-A

69265471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62221790-C-T

69265528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62221743-G-T

69265534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62221737-A-T

69265541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62221730-G-A

69265541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62221730-G-T

69265712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62221561-G-A

69265712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62221561-G-C

69265715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62221558-G-A

69265787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 62221486-G-A

http://identifiers.org/hco/10/GRCh38#69265814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62221459-C-A

69265814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 62221459-C-T

http://identifiers.org/hco/10/GRCh38#69266584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62219725-A-C

69266584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62219725-A-T

69266589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62219720-G-A

69266594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62219715-T-C

69266777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219540-T-C

http://identifiers.org/hco/10/GRCh38#69266855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62219501-C-A

http://identifiers.org/hco/10/GRCh38#69266910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62219475-C-A

69266938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219446-T-C

69267078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219316-G-A

69267078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219316-G-T

http://identifiers.org/hco/10/GRCh38#69267294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62219161-A-C

69267294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219161-A-G

69267294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219161-A-T

http://identifiers.org/hco/10/GRCh38#69267305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62219150-C-A

69267362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219096-A-G

http://identifiers.org/hco/10/GRCh38#69267363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#62219095-A-C

69267364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219094-G-A

69267384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219079-G-A

69267419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62219046-G-A

69267522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62218943-A-G

69267522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62218943-A-T

69267534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23302
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62218931-A-T