47256232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: non coding transcript exon variant
orthologous variants: 16020972-G-A

47256255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: non coding transcript exon variant
orthologous variants: 16020949-A-G

47256439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 16020792-A-G

47256439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 16020792-A-T

47256443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 16020788-G-A

47256443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 16020788-G-T

47256519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 16020713-G-T

47256543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16020689-C-T

47256552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16020680-T-C

47256561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16020671-A-G

47256561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16020671-A-T

47256657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020576-T-A

47256657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020576-T-C

47256657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020576-T-G

47256722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020487-G-C

47256722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020487-G-T

http://identifiers.org/hco/19/GRCh38#47256727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#16020482-A-C

47256727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020482-A-G

47256727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020482-A-T

http://identifiers.org/hco/19/GRCh38#47256736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#16020473-A-C

47256736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020473-A-G

47256736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020473-A-T

47256737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020472-C-G

47256737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020472-C-T

http://identifiers.org/hco/19/GRCh38#47256787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16020425-A-C

47256787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020425-A-G

47256787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020425-A-T

47256799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020411-G-T

47256823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020385-C-T

47256839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020362-C-T

47256854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020347-G-A

47256854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020347-G-C

47256854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020347-G-T

47256896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020305-G-A

47256898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020303-G-A

47256898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020303-G-T

47256953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020210-C-T

47256967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020196-A-G

47257033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020129-T-A

47257033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020129-T-G

http://identifiers.org/hco/19/GRCh38#47257048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#16020113-A-C

47257048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020113-A-G

47257048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020113-A-T

47257051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16020107-G-A

47257078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020052-T-A

47257078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16020052-T-G

47257135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16019975-C-G

47257169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16019907-C-T

47257192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019875-C-T

47257258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019720-A-G

47257294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019655-G-A

47257364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019578-C-T

47257365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019577-G-A

47257399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019536-G-A

47257399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019536-G-T

47257422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16019474-G-C

47257422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16019474-G-T

47257482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16019405-G-T

47257606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16019316-G-A

47257606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16019316-G-T

http://identifiers.org/hco/19/GRCh38#47257648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16019273-C-A

47257708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16019189-A-G

47257719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16019165-G-A

47257746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16019081-C-T

47257825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018956-T-C

47257825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018956-T-G

http://identifiers.org/hco/19/GRCh38#47257864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16018893-A-C

47257909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 16018841-G-A

47257931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018811-G-A

47257931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018811-G-T

47257971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018774-A-G

47258004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018745-G-T

47258026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018727-A-T

47258046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018708-G-T

47258047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018707-T-C

47258047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018707-T-G

47258125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018650-G-A

47258125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018650-G-T

47258127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018648-G-T

http://identifiers.org/hco/19/GRCh38#47258129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16018646-C-A

47258129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018646-C-G

47258129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018646-C-T

http://identifiers.org/hco/19/GRCh38#47258130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16018645-C-A

47258140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018641-A-G

47258148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018633-G-A

47258148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018633-G-T

47258152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018629-A-G

47258172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018614-A-G

47258183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018603-G-A

47258183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018603-G-T

47258203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018576-T-A

47258203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018576-T-G

http://identifiers.org/hco/19/GRCh38#47258261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16018537-C-A

47258261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018537-C-T

47258271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018527-G-A

47258289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018509-G-A

47258289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018509-G-T

47258290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018508-G-A

47258290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 16018508-G-T

47258322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 16018477-G-C

47258322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 16018477-G-T

47258346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5 prime UTR variant
orthologous variants: 16018453-G-A

47258348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5 prime UTR variant
orthologous variants: 16018451-C-T

47258450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018392-G-T

47258505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018351-C-T

47258541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018316-A-G

47258646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 16018211-C-T

47258757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018105-C-T

http://identifiers.org/hco/19/GRCh38#47258813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16018049-C-A

47258813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16018049-C-T

47258857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017988-G-A

47258993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017867-G-A

47259012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017848-A-G

47259063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017802-A-G

47259063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017802-A-T

47259150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017722-G-A

47259297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017616-C-G

47259357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017557-A-G

47259463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017461-G-A

47259680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017264-G-C

47259686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017258-C-T

47259722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017231-C-T

47259942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017103-C-T

47260023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017048-G-A

47260045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16017025-G-C

47260140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016953-C-T

47260147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016944-G-A

47260254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016842-G-T

47260449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016650-C-T

47260454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016645-G-A

47260454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016645-G-T

47260536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016565-C-G

47260536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016565-C-T

http://identifiers.org/hco/19/GRCh38#47260616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16016500-C-A

47260616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 16016500-C-G

47260616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 16016500-C-T

47260662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 16016454-T-C

47260874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016245-G-A

47260920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16016194-T-C

47264579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014884-G-A

47264579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014884-G-T

http://identifiers.org/hco/19/GRCh38#47264675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16014792-C-A

47264675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16014792-C-G

47264675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16014792-C-T

http://identifiers.org/hco/19/GRCh38#47264690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16014777-A-C

47264690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014777-A-G

47264735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014736-G-A

47264740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014731-G-A

47264740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014731-G-C

47264740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014731-G-T

47264761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014705-T-C

http://identifiers.org/hco/19/GRCh38#47264836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16014631-C-A

47264836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16014631-C-G

47264836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16014631-C-T

47264861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16014606-G-A

47264861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16014606-G-T

47264951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014516-G-A

47264951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014516-G-C

47264951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014516-G-T

47264960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014475-G-A

47264960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014475-G-T

47264978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014457-T-C

47265033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014362-G-A

47265033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014362-G-C

47265067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014315-T-C

47265067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014315-T-G

47265073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014309-T-C

http://identifiers.org/hco/19/GRCh38#47265097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16014285-A-C

47265097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014285-A-G

47265097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014285-A-T

47265131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014263-C-G

47265150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014242-T-A

47265150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014242-T-C

47265177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014213-C-G

47265177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014213-C-T

47265201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16014186-A-G

47266558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16012511-G-A

47266558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16012511-G-T

47266572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16012497-G-T

47266840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16012254-C-G

47266840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16012254-C-T

47266878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16012229-C-T

47266936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16012193-G-T

47266937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16012192-A-G

47266985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16012147-G-T

47267004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16012127-G-A

http://identifiers.org/hco/19/GRCh38#47267386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16011428-C-A

47267386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16011428-C-T

47267502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16011308-T-C

47270326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16010776-G-C

47270326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16010776-G-T

http://identifiers.org/hco/19/GRCh38#47270363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16010739-C-A

47270363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16010739-C-T

47270459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16010644-T-C

47270651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16010454-A-T

47270700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010405-C-T

47270771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010365-G-T

http://identifiers.org/hco/19/GRCh38#47270803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16010360-C-A

47270803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010360-C-T

http://identifiers.org/hco/19/GRCh38#47270805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16010358-C-A

47270805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010358-C-G

47270805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010358-C-T

47271029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010249-T-C

47271030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010248-T-A

http://identifiers.org/hco/19/GRCh38#47271124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16010176-C-A

47271124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: synonymous variant
orthologous variants: 16010176-C-T

47271210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010099-G-A

47271210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010099-G-T

47271223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16010086-G-T

47271349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16009922-G-A

47271471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 16009773-T-C

47271513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 16009731-G-C

47271529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: 16009721-C-T

47271602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: 16009648-A-G

47271602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: 16009648-A-T

http://identifiers.org/hco/19/GRCh38#47271644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16009606-C-A

47271644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: 16009606-C-G

47271644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: 16009606-C-T

47271666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: 16009584-T-G

47271872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16009471-T-C

http://identifiers.org/hco/19/GRCh38#47271957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16009392-C-A

47271957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009392-C-G

47271957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009392-C-T

47271959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009390-T-G

47271978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009371-G-C

47271978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009371-G-T

47272023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009343-G-A

47272024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009342-A-G

47272070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 16009297-A-G

47272070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 16009297-A-T

47272087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: missense variant
orthologous variants: 16009280-C-T

47272124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: synonymous variant
orthologous variants: 16009243-C-T

47272240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009133-G-A

47272240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009133-G-C

47272240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009133-G-T

47272296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009079-T-A

47272296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009079-T-C

47272296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009079-T-G

47272326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16009054-C-T

47272393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16008992-T-A

47272471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16008945-A-G

47272820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16008730-C-G

47272872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, undefined
orthologous variants: 16008682-A-G

47272933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16008624-A-T

47273008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16008591-G-A

47273296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron variant
orthologous variants: 16008394-G-A

http://identifiers.org/hco/19/GRCh38#47273437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#16008259-C-A

47273437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: intron_variant, missense_variant
orthologous variants: 16008259-C-T

47273492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16008206-T-C

47273550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16008163-G-A

47273550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16008163-G-T

47273605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16008109-A-G

47273611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16008103-G-A

47273611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16008103-G-T

47273655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16008069-G-T

47273656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16008068-G-A

47273656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16008068-G-T

47273657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16008067-A-T

47273660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16008064-G-A

47273660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16008064-G-T

47273662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 16008062-T-C

47273717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24560
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16008054-T-C