http://identifiers.org/hco/9/GRCh38#19409052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86792694-C-A

19409052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86792694-C-T

http://identifiers.org/hco/9/GRCh38#19409159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86792800-C-A

19409159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86792800-C-T

http://identifiers.org/hco/9/GRCh38#19409342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86792956-C-A

19409342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86792956-C-T

19409454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86793060-C-T

19409465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86793070-C-T

19409498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793104-T-C

http://identifiers.org/hco/9/GRCh38#19409687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86793313-C-A

19409687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793313-C-T

http://identifiers.org/hco/9/GRCh38#19409850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86793433-A-C

19409850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86793433-A-G

19409850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86793433-A-T

19409966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793542-G-A

19409966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793542-G-C

19409966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793542-G-T

http://identifiers.org/hco/9/GRCh38#19409993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86793569-C-A

19410145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793724-A-T

19410157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793743-G-C

http://identifiers.org/hco/9/GRCh38#19410702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86793983-A-C

19410713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86793992-C-G

19410900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86794171-A-G

19410902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86794174-A-G

19411020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86794278-C-T

http://identifiers.org/hco/9/GRCh38#19411828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86795335-C-A

19411828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86795335-C-T

19411961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86795448-G-A

19411961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86795448-G-C

19411982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86795469-G-A

19412138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86795596-C-T

19413636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86797666-C-G

http://identifiers.org/hco/9/GRCh38#19413698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86797726-C-A

19413698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86797726-C-T

19413717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86797745-C-T

19413772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86797788-G-A

19413858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86797879-G-A

http://identifiers.org/hco/9/GRCh38#19413897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86797919-C-A

19413897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86797919-C-T

19413994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798007-A-G

19414025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798037-T-C

19414167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798601-G-A

19414210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798641-C-G

19414210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798641-C-T

19414271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798692-A-G

19414333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798744-G-A

19414747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86798974-A-G

19414896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86799021-A-G

19414932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86799062-G-A

19414932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86799062-G-C

19414956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86799087-T-C

19414983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86799113-A-G

http://identifiers.org/hco/9/GRCh38#19415022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86799152-A-C

19420117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86800475-G-A

19420131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86800490-C-G

19420131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86800490-C-T

19420328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86801950-G-C

19420367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86801990-A-G

19420392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802015-G-A

19420412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802022-T-C

19420479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802090-C-T

19420629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802225-A-G

19420641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802237-G-A

19420708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802307-A-G

19420730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802325-C-T

19420731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86802326-A-G

19422496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86803882-C-T

19422551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86803938-G-T

19423727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86804263-A-G

http://identifiers.org/hco/9/GRCh38#19423738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86804273-A-C

19423738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86804273-A-T

http://identifiers.org/hco/9/GRCh38#19423758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86804293-C-A

http://identifiers.org/hco/9/GRCh38#19423771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86804306-A-C

19423805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86804341-A-G

19423921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 86804454-T-A

19423921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86804454-T-C

http://identifiers.org/hco/9/GRCh38#19423996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86804529-A-C

19424068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86804587-A-G

19424209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86804726-A-G

19424401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86804922-T-G

19424455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86804976-G-C

19424484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86805005-G-T

19424545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86805066-G-T

19424628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86805190-A-G

19424728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86805289-C-G

19424728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86805289-C-T

19424846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86805407-G-A

19424906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86805455-T-C

19424946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86805494-T-G

19424957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86805505-T-C

19425001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86805545-A-G

19425070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86805603-T-C

19426556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809550-T-C

19426556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809550-T-G

19426631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809619-A-G

19426643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809631-A-G

19426655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809643-A-G

19426861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809796-A-G

19426900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809818-A-T

19426918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809834-G-C

19427007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809854-C-T

19427101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86809938-A-G

19427350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86810110-A-T

http://identifiers.org/hco/9/GRCh38#19427429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86810185-A-C

19427429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86810185-A-G

19427678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86810319-T-C

19427699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86810331-C-G

19429712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86815158-A-G

19429757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86815200-G-A

19430219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86815481-A-T

19430353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86815610-T-C

19430379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86815635-G-C

19430444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86815680-G-A

19430571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86815816-T-A

19431325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86816302-G-A

19431343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86816313-G-C

19431567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817099-A-G

19431813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817330-C-T

http://identifiers.org/hco/9/GRCh38#19432008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86817518-C-A

19432115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817627-C-G

19432115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817627-C-T

19432164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817648-G-T

19432277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817743-A-G

19432277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817743-A-T

http://identifiers.org/hco/9/GRCh38#19432281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86817747-C-A

19432281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817747-C-G

19432329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817792-G-A

19432401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817867-G-A

19432401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817867-G-T

19432491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817929-T-C

19432492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817930-C-G

19432492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86817930-C-T

19432811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818058-C-G

19432872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818107-G-A

19432884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818119-A-G

19432926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818146-T-C

19432995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818196-G-A

19433109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818280-T-G

19433115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818286-G-A

19433115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818286-G-T

19434918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86818691-T-C

19434996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86818768-C-T

19435001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86818773-A-G

19435005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86818777-G-A

19435005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86818777-G-T

19435013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86818785-T-C

19435067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86818839-C-T

http://identifiers.org/hco/9/GRCh38#19441444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86820292-C-A

http://identifiers.org/hco/9/GRCh38#19441478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86820330-A-C

19441741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86820577-T-C

19441741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86820577-T-G

19441742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86820578-C-T

19441858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86820693-G-C

http://identifiers.org/hco/9/GRCh38#19441872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86820707-A-C

19441872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86820707-A-G

19442481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86822498-A-G

19442521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86822540-C-T

19442590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86822565-C-T

19444872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86824625-A-G

19444899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86824654-G-T

19444920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86824691-C-T

19445609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829277-C-T

http://identifiers.org/hco/9/GRCh38#19445764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86829411-C-A

19445764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829411-C-T

19445934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829551-G-A

19445934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829551-G-T

19446021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829627-T-A

19446021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829627-T-G

19446048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829653-T-A

19446063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829668-A-G

19446078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86829677-G-T

http://identifiers.org/hco/9/GRCh38#19446446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86830022-C-A

19446446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830022-C-G

19446446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830022-C-T

19446533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830134-T-C

19446588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86830178-A-G

http://identifiers.org/hco/9/GRCh38#19446589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86830179-A-C

19446688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830276-C-G

19446690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830278-A-G

19446714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830302-T-A

19446733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830316-G-A

19446774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830356-G-A

19446774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830356-G-T

19446791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830372-G-A

19446856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830437-G-A

19446908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830488-C-T

19446909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830489-A-G

19447031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830591-A-G

19447788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86830897-A-G

19450223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 86835453-G-C

19450257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86835482-T-C

19450495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: synonymous variant
orthologous variants: 86835676-T-C

http://identifiers.org/hco/9/GRCh38#19450585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86835766-C-A

19450585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: synonymous variant
orthologous variants: 86835766-C-T

19450680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86835865-A-G

http://identifiers.org/hco/9/GRCh38#19451011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86835963-C-A

19451011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86835963-C-G

19451011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86835963-C-T

19451056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86835988-T-C

http://identifiers.org/hco/9/GRCh38#19451107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86836037-C-A

19451107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836037-C-T

19451120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836050-G-T

19451121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836051-G-A

19451121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836051-G-T

19451139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836069-A-G

http://identifiers.org/hco/9/GRCh38#19451165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86836095-C-A

19451172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836102-G-A

19451172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836102-G-T

http://identifiers.org/hco/9/GRCh38#19451215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86836139-C-A

19451215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836139-C-T

19451267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836163-C-G

19451267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836163-C-T

19451293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836189-T-C

http://identifiers.org/hco/9/GRCh38#19451363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86836264-A-C

http://identifiers.org/hco/9/GRCh38#19451364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86836265-C-A

19451385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836286-G-T

19451503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836397-T-C

http://identifiers.org/hco/9/GRCh38#19451589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86836444-A-C

19451729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836566-C-G

19451729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836566-C-T

19451738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836575-G-T

19451899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836761-T-C

19451943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86836797-T-C

http://identifiers.org/hco/9/GRCh38#19452214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86837015-C-A

19452271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 86837079-G-A

19452374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23675
most severe consequence: 3 prime UTR variant
orthologous variants: 86837172-C-G