http://identifiers.org/hco/10/GRCh38#11742412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6217818-C-A

11742412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6217818-C-G

11742412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6217818-C-T

http://identifiers.org/hco/10/GRCh38#11742582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6217764-C-A

11742582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6217764-C-G

11742582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6217764-C-T

11742609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6217737-G-A

11742609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6217737-G-C

11742609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6217737-G-T

11742610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6217736-G-A

11742610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6217736-G-C

11742610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6217736-G-T

11742625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6217721-T-A

11742625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6217721-T-C

11742625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6217721-T-G

http://identifiers.org/hco/10/GRCh38#11742654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6217692-C-A

11742654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6217692-C-T

http://identifiers.org/hco/10/GRCh38#11742723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6217623-C-A

11742723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6217623-C-G

11742723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6217623-C-T

http://identifiers.org/hco/10/GRCh38#11742754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6217591-C-A

11742754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6217591-C-T

11742856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6217462-G-A

11742856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6217462-G-C

11742856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 6217462-G-T

http://identifiers.org/hco/10/GRCh38#11742881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6217421-C-A

11742881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 6217421-C-T

http://identifiers.org/hco/10/GRCh38#11742950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6217357-C-A

11742950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6217357-C-T

11743095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6217188-G-A

11743194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6217092-G-A

11743330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6217002-A-G

11743494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6216850-C-G

http://identifiers.org/hco/10/GRCh38#11743495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6216849-A-C

11743509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6216835-C-G

11743541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6216818-C-T

http://identifiers.org/hco/10/GRCh38#11743724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6216646-C-A

11743724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6216646-C-T

11743811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6216379-C-G

http://identifiers.org/hco/10/GRCh38#11743921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6216136-C-A

11743942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6216115-T-G

11743968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6216093-A-T

11744152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215920-T-G

11744196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215880-A-G

11744218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215860-C-T

11744385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215723-A-T

11744601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215596-G-A

11744619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215578-C-G

11744619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215578-C-T

11744632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215565-A-G

11744693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215515-G-A

11744999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215223-C-T

11745057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215165-A-G

11745155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215076-G-A

11745155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6215076-G-C

11745261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6214995-C-G

11745329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6214740-G-T

http://identifiers.org/hco/10/GRCh38#11745722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6214241-C-A

11745728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6214235-G-A

11745728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6214235-G-C

11745905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6214064-C-T

11747000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6213766-G-T

11747102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6213667-A-G

11747127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6213630-G-T

11747183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6213565-T-A

http://identifiers.org/hco/10/GRCh38#11747207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6213539-A-C

11747433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6213314-C-T

11747505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6213242-G-T

11747550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6213192-T-C

11747550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6213192-T-G

11747823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6212729-G-T

11748021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211917-A-T

11748042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211896-A-G

11748189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211763-G-A

11749553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6211263-C-T

http://identifiers.org/hco/10/GRCh38#11749583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6211233-C-A

11749583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6211233-C-G

11749662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211154-C-T

11749704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211113-A-G

11749705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211112-G-C

11749705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211112-G-T

11749710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211102-A-T

11749737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211080-T-A

11749737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6211080-T-C

11750119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6210679-C-T

11750141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6210657-T-C

11750181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6210626-G-C

11750947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6210096-G-C

11751022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6209681-G-A

11751022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6209681-G-C

11751029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6209674-G-T

11751120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6209583-A-G

11751262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6209471-G-A

11751349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6209384-G-A

11751483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6209042-C-T

11751537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208987-G-A

11751616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208907-T-A

11751640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208884-A-G

11751641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208883-T-C

11751940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208599-G-A

11751966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208574-C-T

11752095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208454-A-G

11752103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208446-A-G

11752103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208446-A-T

11752151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208406-G-A

11752151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208406-G-T

11752185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208377-C-T

11752237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208333-G-A

11752237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208333-G-T

11752238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208332-A-G

11752238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208332-A-T

11752245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208326-G-A

11752245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6208326-G-T

11752607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208131-T-A

11752607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208131-T-G

11752641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208093-T-C

11752643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208091-G-A

11752683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6208050-C-T

11752786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6207947-A-G

11753133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6207645-C-T

11753151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6207628-T-C

11753193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6207602-C-T

11753587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6206801-C-G

11753587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6206801-C-T

11754334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6201345-G-A

11754550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6201087-G-A

http://identifiers.org/hco/10/GRCh38#11755231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6200648-C-A

11755231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200648-C-T

11755237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200642-G-A

11755237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200642-G-T

http://identifiers.org/hco/10/GRCh38#11755238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6200641-A-C

11755238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200641-A-G

11755238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200641-A-T

11755239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200640-T-A

11755239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200640-T-C

11755239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200640-T-G

11755241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200638-G-A

11755241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200638-G-C

11755241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6200638-G-T

11755387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6200613-G-T

11755394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6200606-T-C

http://identifiers.org/hco/10/GRCh38#11755401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6200599-C-A

11755401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6200599-C-G

http://identifiers.org/hco/10/GRCh38#11755423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6200577-C-A

11755423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6200577-C-T

11755573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6200427-C-T

http://identifiers.org/hco/10/GRCh38#11755625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6200375-C-A

11755625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6200375-C-T

http://identifiers.org/hco/10/GRCh38#11755819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6199932-A-C

11755824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199927-A-G

11755824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199927-A-T

11755842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199909-T-A

11755842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199909-T-G

http://identifiers.org/hco/10/GRCh38#11755864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6199886-A-C

11755864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199886-A-G

11755864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199886-A-T

http://identifiers.org/hco/10/GRCh38#11755869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6199881-C-A

11755869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199881-C-G

http://identifiers.org/hco/10/GRCh38#11755870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6199880-A-C

11755870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199880-A-G

11755870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199880-A-T

http://identifiers.org/hco/10/GRCh38#11756109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6199657-A-C

11756328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199443-G-T

11756587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199203-G-A

11756587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199203-G-C

11756614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199180-G-A

11756624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199170-A-G

11756642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199155-G-A

11756703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6199097-G-A

http://identifiers.org/hco/10/GRCh38#11757437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6198696-C-A

11757674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6198491-G-A

11757674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6198491-G-T

11757692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6198473-A-G

11758041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6198056-C-T

11758049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6198049-G-A

http://identifiers.org/hco/10/GRCh38#11758249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6197849-C-A

11758314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6197787-G-A

http://identifiers.org/hco/10/GRCh38#11758336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6197766-C-A

11758533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6197548-G-A

11758933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6197280-C-T

11758943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6197272-C-T

11759026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6197188-G-C

11759063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6197154-C-T

http://identifiers.org/hco/10/GRCh38#11762417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6195245-C-A

11762439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6195237-G-A

11762454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6195223-G-T

11762600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6195098-G-T

11762712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6194991-C-G

11762742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6194966-A-G

http://identifiers.org/hco/10/GRCh38#11762927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6194797-C-A

11762967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6194759-C-T

11763052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6194672-C-T

11763069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6194655-G-A

http://identifiers.org/hco/10/GRCh38#11763083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6194641-C-A

11763190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6194495-G-A

11763190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6194495-G-T

http://identifiers.org/hco/10/GRCh38#11763287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6194397-C-A

11763287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6194397-C-T

11763310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6194374-G-C

11763310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6194374-G-T

11763314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6194370-G-A

11763351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6194333-T-A

11763351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6194333-T-G

11763383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6194301-G-T

11763461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6194223-A-G

http://identifiers.org/hco/10/GRCh38#11763468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6194216-C-A

11763468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6194216-C-T

11763544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 6194139-A-T

http://identifiers.org/hco/10/GRCh38#11763622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6194054-C-A

11763622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6194054-C-T

11763726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193951-G-C

11763726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193951-G-T

11763814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193874-G-A

11763814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193874-G-T

http://identifiers.org/hco/10/GRCh38#11763831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6193857-C-A

11763831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193857-C-G

11763831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193857-C-T

http://identifiers.org/hco/10/GRCh38#11763848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6193847-A-C

http://identifiers.org/hco/10/GRCh38#11763884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6193810-C-A

http://identifiers.org/hco/10/GRCh38#11763892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6193802-A-C

11763892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193802-A-G

11763902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193794-G-A

11763902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193794-G-C

11763986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6193708-A-G