72782211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337427-G-T

72782220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337436-G-C

http://identifiers.org/hco/13/GRCh38#72782223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337439-C-A

http://identifiers.org/hco/13/GRCh38#72782235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337452-A-C

http://identifiers.org/hco/13/GRCh38#72782258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337474-C-A

72782258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337474-C-G

72782258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337474-C-T

72782266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337481-T-A

72782266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337481-T-C

72782266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337481-T-G

72782284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99337499-T-A

72782284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99337499-T-C

72782284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99337499-T-G

http://identifiers.org/hco/13/GRCh38#72782366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337582-A-C

http://identifiers.org/hco/13/GRCh38#72782389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337608-C-A

72782444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99337661-G-C

72782444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99337661-G-T

72782507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99337726-T-G

72782570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99337792-C-T

http://identifiers.org/hco/13/GRCh38#72782770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337998-C-A

72782770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99337998-C-G

72783070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338146-C-G

72783376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338411-G-A

72783391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338432-G-A

72783391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338432-G-T

72783691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99338707-C-G

72783691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99338707-C-T

72784486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338809-C-G

72784486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338809-C-T

72784493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338816-T-C

72784494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99338817-C-T

72791415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99341912-G-T

72791483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99341979-A-G

72791512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99342004-T-C

72792517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99342675-A-G

72792587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99342742-T-A

72792587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99342742-T-C

72792587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99342742-T-G

72792646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99342801-A-G

72792646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99342801-A-T

72792713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99342865-G-T

72795000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99344204-A-G

http://identifiers.org/hco/13/GRCh38#72795102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99344541-A-C

72795225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99344653-T-A

72795675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348154-A-G

72795878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348479-G-C

72796111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348671-A-T

http://identifiers.org/hco/13/GRCh38#72796171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99348876-A-C

72796208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348897-A-G

72796233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348918-A-T

72796281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348967-G-A

72796282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99348968-T-C

72796322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349005-G-A

72796354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349037-T-C

72796490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349159-G-A

72796699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349358-A-G

72796699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349358-A-T

72796702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99349361-C-T

http://identifiers.org/hco/13/GRCh38#72796724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99349378-C-A

72797438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99350021-G-A

http://identifiers.org/hco/13/GRCh38#72797903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99350402-C-A

72797903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99350402-C-T

72797933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99350432-A-G

72797950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99350449-G-C

72798077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99350576-G-C

72798698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351097-T-C

72805446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99351640-G-A

72805975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99352148-A-G

72806094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99352266-T-C

72809009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99355157-C-G

72809060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99355183-G-A

72809325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99355388-G-A

72809405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99355472-A-G

72811675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99356139-A-G

72811718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99356170-G-A

72811824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99356268-C-T

72811860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99356305-G-T

72811892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99356340-G-A

72812100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99356690-G-A

72814504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99358395-A-G

72814672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99358537-A-G

72815227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99359178-T-A

72815465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99359509-A-G

72816944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99362762-A-G

72817179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99363002-C-G

72817179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99363002-C-T

72817253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99363073-A-G

72817335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99365218-T-A

72817497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99365367-C-T

72817788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99365596-A-G

72817823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99365637-G-C

72817850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99365663-A-G

72817855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99365668-A-G

72819963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99369751-A-G

72819985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99369779-A-G

72820149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99369913-T-C

72820157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99369915-A-T

72820272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370015-C-T

72820379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370107-G-A

72820415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370150-G-A

http://identifiers.org/hco/13/GRCh38#72820482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99370217-C-A

72820482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370217-C-T

72820644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370391-T-C

72821634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370429-T-A

72821737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370543-T-C

72821881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99370704-A-G

72821989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99370812-A-G

http://identifiers.org/hco/13/GRCh38#72822014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99370834-C-A

72822024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370843-A-G

http://identifiers.org/hco/13/GRCh38#72822041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99370860-C-A

72822041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370860-C-T

72822068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370888-T-A

72822068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370888-T-G

72822104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370915-G-A

72822104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370915-G-T

http://identifiers.org/hco/13/GRCh38#72822105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99370916-C-A

72822105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370916-C-G

72822146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370931-A-G

72822174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99370959-G-A

http://identifiers.org/hco/13/GRCh38#72822181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99370966-C-A

72823135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99371532-A-G

72823146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99371543-A-G

72823257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99371642-G-A

72823525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99372081-G-A

72823598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99372139-A-G

72823608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99372149-A-G

72823826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99372319-G-A

72825960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99372837-C-T

72826114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99372986-T-A

72826662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373508-A-G

72826675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373521-C-T

http://identifiers.org/hco/13/GRCh38#72826686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99373562-A-C

72826706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373582-A-G

72826901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373799-A-G

72826931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373822-A-T

http://identifiers.org/hco/13/GRCh38#72826941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99373828-C-A

72826941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373828-C-T

http://identifiers.org/hco/13/GRCh38#72826943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99373830-C-A

72826943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373830-C-T

http://identifiers.org/hco/13/GRCh38#72826989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99373869-C-A

72826989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99373869-C-G

72827094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99373973-A-G

72827128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374007-T-C

72827157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374036-A-G

72827646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374408-A-G

72827705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374463-G-A

72827705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374463-G-C

72827705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374463-G-T

72827804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99374549-G-A

72827804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99374549-G-C

72827804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99374549-G-T

72827807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99374552-T-C

http://identifiers.org/hco/13/GRCh38#72827925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99374668-C-A

72827925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99374668-C-T

72827940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374682-A-G

72827940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374682-A-T

http://identifiers.org/hco/13/GRCh38#72827956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99374698-A-C

72827956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374698-A-G

72828059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374771-T-C

72828091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99374801-C-T

72834322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99377508-A-G

72835222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99377954-G-A

72835360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99378090-A-G

72836151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99378492-G-C

http://identifiers.org/hco/13/GRCh38#72836168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99378509-C-A

72836168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99378509-C-T

http://identifiers.org/hco/13/GRCh38#72836240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99378578-C-A

72836240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99378578-C-T

72836244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99378582-T-C

72836255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99378595-G-C

72836255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99378595-G-T

72839948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99379805-T-G

72840185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99380011-T-C

72840224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99380051-T-A

72841423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99380722-A-G

http://identifiers.org/hco/13/GRCh38#72841440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99380737-A-C

72842226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381088-A-G

72842284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381150-T-C

72842317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381175-T-C

72842392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381243-A-T

72842399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381250-A-G

72842401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381251-A-G

72842401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381251-A-T

72842425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381280-A-G

72842425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381280-A-T

72842459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381307-A-G

http://identifiers.org/hco/13/GRCh38#72842572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99381413-C-A

72842679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381527-T-C

72842735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381578-A-G

72842982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381807-A-G

72847000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99381941-A-G

72847127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99382054-C-T

72847381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99382486-A-G

72847430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99382535-A-G

72847510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99382628-A-G

72847546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99382662-T-C

72847603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99382719-A-G

72848280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99382947-T-A

72849683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99384450-A-G

72849811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99384579-T-C

72849903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99384662-G-A

72850117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99385538-G-C

72850474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99386104-T-C

72852829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99386774-T-G

72852836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99386781-G-T

72852932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99386877-C-T

72853102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387048-G-T

72853129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387074-C-T

72853164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387097-C-G

72853192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387125-T-A

72853388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387302-A-G

http://identifiers.org/hco/13/GRCh38#72853496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99387502-A-C

72853590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387584-T-C

72853625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387618-T-A

72853727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387718-A-G

72853727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99387718-A-T

http://identifiers.org/hco/13/GRCh38#72853809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99387787-A-C

72854123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99388145-T-C

72862308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99397607-G-A

http://identifiers.org/hco/13/GRCh38#72862589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99398215-A-C

72863014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99398587-G-T

72863025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99398599-T-C

72863731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99399413-A-G

72863837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99399623-G-A

72863837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99399623-G-T

72863990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99399839-C-T

72864161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99400054-C-T

72864343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99400236-A-G

72864768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99400607-G-A

72864799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99400638-A-T

72865125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99400957-G-A

72865205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99401030-T-C

72865252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99401076-T-G

72865287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99401112-G-A

72865513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99401459-A-G

72865559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99401503-G-A

72866018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99402429-G-T

72866210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99402603-C-G

72867706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99405434-C-T

http://identifiers.org/hco/13/GRCh38#72867766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99405493-A-C

72868509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99405599-T-C

72868513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99405603-A-G

72868731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99405913-C-T

72868786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99405987-C-G

72868786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99405987-C-T

72868804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99406005-T-G

http://identifiers.org/hco/13/GRCh38#72868808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99406009-A-C

72868851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99406077-A-G

72868851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99406077-A-T

72868854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99406080-T-A

72868854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99406080-T-G

72870084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99407465-A-G

72870099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99407482-A-G

72870143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99407712-A-G

72870359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99407911-C-T

72870420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99407967-A-G

72870448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99407992-T-C

72885253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99408261-T-C

72886215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99409353-G-A

72886336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99409630-G-A

72886336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99409630-G-T

72886689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99409959-A-G

http://identifiers.org/hco/13/GRCh38#72887122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99410316-C-A

72887122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99410316-C-T

72887721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99410721-T-A

72887815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99410797-T-C

72888076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99411024-G-C

72888092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99411042-G-C

72888200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99411189-T-C

72888382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99411459-G-A

72888615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99411867-T-G

72888622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99411874-A-G

72889209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99412281-G-A

72889220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99412292-T-C

http://identifiers.org/hco/13/GRCh38#72889225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99412297-A-C

72889944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99412915-G-A

72890278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99413513-T-C

72890279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99413514-A-G

72890295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99413546-A-G

72890557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99413834-C-T

72890713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414143-C-G

72890713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414143-C-T

72891075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414514-C-T

72891424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99415026-T-C

72891528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99415127-C-T

72892848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416106-G-A

72893048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416299-A-T

72893080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416329-C-T

72893212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416457-G-A

72893656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416591-G-A

72893656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416591-G-C

72893656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416591-G-T

http://identifiers.org/hco/13/GRCh38#72893735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99416672-C-A

72893735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416672-C-T

72893886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99416853-G-A

72893980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416947-G-A

72894026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99416992-T-C

http://identifiers.org/hco/13/GRCh38#72894045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99417010-C-A

http://identifiers.org/hco/13/GRCh38#72894072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99417037-A-C

72894091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99417097-G-A

72894091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99417097-G-T

72908691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99424085-C-G

http://identifiers.org/hco/13/GRCh38#72908696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99424090-A-C

72908700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99424094-A-G

72908714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99424108-T-C

72916836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99424935-C-G

http://identifiers.org/hco/13/GRCh38#72916996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99425078-C-A

72917065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99425143-A-G

http://identifiers.org/hco/13/GRCh38#72917175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99425253-A-C

72917175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99425253-A-G

72917184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99425262-T-A

72917184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99425262-T-C

72918289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99426522-C-G

72918289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99426522-C-T

72920854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99428170-A-T

72920906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99428217-C-T

72921040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99428349-G-A

72921446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99428405-A-G

72921489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99428448-T-C

72922449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99429891-A-G

72922484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99429917-A-G

http://identifiers.org/hco/13/GRCh38#72922496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99429928-A-C

72922496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99429928-A-G

72929007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99430551-A-T

72929146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99430688-A-G

72929760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99431791-A-G

72930665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433254-A-G

72930912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433553-G-A

72931084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433702-T-G

72931316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433930-A-G

72931394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99434014-G-A

72931408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99434028-G-A

72931408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99434028-G-T

72931474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99434089-C-T

72955288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99440119-A-G

72955954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99440593-C-G

72956042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99440664-G-A

72956571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99441028-G-A

72958493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99442405-G-A

72958682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99442593-G-A

72959525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443015-C-T

72959576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443074-G-A

72959614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443112-A-G

72959717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443347-G-A

72959728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443359-T-A

72959862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443483-C-T

72959957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443576-A-G

72960608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99444201-T-G

72960612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99444214-C-G

72960722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99444328-A-T

72960826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99444409-C-G

72960826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99444409-C-T

72960872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99444452-A-G

72960890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99444470-A-T

72965181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448286-G-T

72965197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448298-T-C

72965197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448298-T-G

http://identifiers.org/hco/13/GRCh38#72965366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#99448468-A-C

72965404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 99448506-G-A

72965419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99448521-A-G

72965419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99448521-A-T

72965469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448568-T-A

72965469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448568-T-C

72965470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448569-G-A

72965470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448569-G-T

http://identifiers.org/hco/13/GRCh38#72965518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99448613-C-A

72965518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448613-C-G

72965710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449066-G-A

72965947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449282-A-G

72966463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99450503-C-T

72968503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454225-G-A

72968503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454225-G-C

72968512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454234-G-A

72968544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454286-G-A

72968544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454286-G-T

http://identifiers.org/hco/13/GRCh38#72968561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99454303-A-C

72968581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454322-A-G

72968759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454507-C-T

72969531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455246-T-G

72970102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455749-T-G

72970158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455854-T-C

72970229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455926-C-T

http://identifiers.org/hco/13/GRCh38#72970315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99456006-C-A

72970325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456016-A-T

72970348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456043-A-G

72970391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456085-A-G

72970392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456086-T-C

72970483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456185-A-T

72970722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456423-G-A

72970813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456646-A-G

72970849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456690-C-T

72971189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457016-T-A

72971189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457016-T-C

72971323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457115-A-G

72971455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457242-C-T

72971920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457698-T-C

72971933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457711-C-T

72972981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99458283-C-T

72973568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99458975-A-T

72973627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99459031-G-A

72973672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99459076-T-C

72973681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99459085-T-C

72973692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99459095-G-A

72973692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99459095-G-C

72973692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99459095-G-T

72973693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 99459096-T-C

72973712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99459116-A-G

72973713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99459117-G-T

http://identifiers.org/hco/13/GRCh38#72973730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99459137-C-A

72973730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99459137-C-G

72973733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99459139-T-A

72973733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99459139-T-C

http://identifiers.org/hco/13/GRCh38#72973763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99459171-C-A

72973763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99459171-C-T

72973801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99459206-T-A

http://identifiers.org/hco/13/GRCh38#72973867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99459275-C-A

72973994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99459403-A-T

72974887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460887-A-G

http://identifiers.org/hco/13/GRCh38#72974894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99460894-A-C

72975440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99461145-A-G

72975457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99461352-G-A

http://identifiers.org/hco/13/GRCh38#72975731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99462165-C-A

72975731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99462165-C-G

72975731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99462165-C-T

72975777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99462211-T-C

72977129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99462717-A-G

72977686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99462884-G-A

72977712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99462910-C-G

72978190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463445-G-A

72978355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463616-G-A

72978590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463873-G-T

72978667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463948-T-G

72978669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463950-C-T

72978697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463978-A-G

72980426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99465463-C-T

72982937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99466730-G-A

72983343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99466843-T-C

72983365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99466862-C-T

72983439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99466936-G-A

72983446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99466943-G-A

72983470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99466965-C-G

72983516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99467009-C-T

72984072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99467602-A-G

72984536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468584-C-G

72984544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468591-C-G

http://identifiers.org/hco/13/GRCh38#72984756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99468809-C-A

72984823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468882-C-T

http://identifiers.org/hco/13/GRCh38#72984985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99469048-C-A

72984985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469048-C-T

72985780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469790-A-G

72985789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469799-A-G

72985797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469807-A-G

72985829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469845-A-G

72987116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470539-A-G

72987156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470580-G-T

72987177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470601-G-A

72987177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470601-G-T

72987388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470756-G-A

72987388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470756-G-T

72987394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470762-A-G

72987403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470771-G-A

72990743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474326-G-A

72990747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474330-C-T

72990762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474347-C-T

72990787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474369-G-A

72990823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474392-G-T

72991221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474839-T-G

72991458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99475168-G-A

72993777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99475771-T-A

72993842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99475835-A-G

72994354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99477170-G-T

72996889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99477813-C-T

72997394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99478475-A-G

72997719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99478755-G-A

72997719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99478755-G-T

http://identifiers.org/hco/13/GRCh38#72997930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99478913-C-A

72998147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99479518-A-G

72998224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99479658-A-G

72998246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99479680-G-A

72998248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99479682-T-G

72998261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99479695-G-A

72998675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480113-G-A

72998675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480113-G-T

http://identifiers.org/hco/13/GRCh38#72998676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99480114-C-A

72998676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480114-C-T

72998677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480115-A-G

72998766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480221-T-C

72999052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480500-T-C

72999052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480500-T-G

72999114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480551-A-G

72999136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480573-T-G

73002193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99482647-G-T

73002299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99482745-G-A

73006529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99483183-T-G

73007875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484305-C-G

73008019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484473-G-A

73008467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99485107-A-G

73008614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99485218-A-G

http://identifiers.org/hco/13/GRCh38#73015902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99491630-C-A

73015941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491669-G-A

73015942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491670-T-C

73015953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491725-A-G

73015975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491747-G-A

73015975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491747-G-T

73016088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491866-A-G

http://identifiers.org/hco/13/GRCh38#73016092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99491870-A-C

73016092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491870-A-G

73016092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491870-A-T

73016133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99491919-A-G

73016381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99492474-T-G

http://identifiers.org/hco/13/GRCh38#73016428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23352
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99492524-C-A