127229500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 57218503-G-A

127229500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57218503-G-T

127229533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57218549-C-T

127229544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57218560-G-A

127229562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57218578-C-T

http://identifiers.org/hco/5/GRCh38#127229593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57218616-C-A

127229593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57218616-C-T

127229595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57218618-G-A

127229595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57218618-G-C

127229595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57218618-G-T

127229597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57218636-T-C

127229599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57218638-G-T

127229605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57218644-A-G

127229605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57218644-A-T

127289567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57265432-G-C

127289604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57265475-C-T

127289700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57265593-C-T

127289846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57265713-T-C

127290051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57265876-G-A

127290642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57266372-G-T

127290676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57266421-G-C

127290694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57266448-A-G

127290851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 57266604-T-C

127290851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 57266604-T-G

127290905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 57266648-G-C

127290905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 57266648-G-T

127291012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 57266759-G-A

127291012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 57266759-G-T

127291074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, missense_variant
orthologous variants: 57266816-T-C

127291082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57266824-G-A

http://identifiers.org/hco/5/GRCh38#127291361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57267086-C-A

127291400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57267127-T-C

127291426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57267149-C-T

127292131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57267833-G-A

127293046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57268607-A-G

http://identifiers.org/hco/5/GRCh38#127293203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57268787-A-C

127293495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57269035-T-A

127293510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57269050-G-A

127293878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57269329-C-T

127293923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57269376-A-G

127293936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57269386-G-T

127294285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57269695-G-A

127294935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57269978-C-T

127294992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57270032-G-A

127295184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57270209-T-C

http://identifiers.org/hco/5/GRCh38#127295504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57270513-C-A

127295504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57270513-C-T

127295587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57270563-T-C

127295724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57270693-A-T

127295917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57270854-T-C

127295995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57270908-A-G

127296165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57271041-A-G

127296432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, undefined
orthologous variants: 57271306-C-T

http://identifiers.org/hco/5/GRCh38#127297727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57273289-C-A

127297922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57273481-A-G

127297924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57273483-G-A

127298239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274056-G-C

127298334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274174-G-T

127298539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274343-T-C

127298620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274397-T-C

127298752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274532-C-G

127298863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274643-A-G

127298906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274686-G-A

127299016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57274793-C-G

127299381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57275410-T-C

127300150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57276165-G-A

127300150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57276165-G-T

127300273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57276290-G-A

127300346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57276367-G-T

127300365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57276387-G-T

http://identifiers.org/hco/5/GRCh38#127300484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57276563-C-A

127300775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57276862-C-T

127300794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57276875-C-T

127301055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277108-C-T

127301326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277455-A-T

127301390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277520-A-T

127301479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277603-C-G

127301536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277658-G-T

127301628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277745-G-A

127301676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277790-T-C

127301676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57277790-T-G

127302061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278159-A-G

127302061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278159-A-T

127302090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278198-G-T

127302232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278334-C-T

127302312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278401-A-G

127302373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278450-A-G

127302388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278465-G-T

127302462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278541-G-C

127302725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278794-A-G

127302877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57278912-C-T

127303002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57279039-A-G

127303005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57279042-G-C

127303446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57279375-A-G

127303465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57279394-G-A

127303693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57280683-A-G

127303912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57280895-A-G

127303913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57280896-T-C

127303947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57280924-C-G

127304247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57281214-C-G

127304247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57281214-C-T

127305157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57284025-C-T

127305608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57284394-T-A

127305659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57284433-G-A

127306200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57284934-G-A

127306279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285160-A-G

127306435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285408-C-G

127306435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285408-C-T

127306445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285418-G-T

127306517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285484-C-T

127306526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285488-T-C

127306678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285655-G-A

127306816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285783-C-T

127306824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285791-A-G

127306961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57285914-C-T

http://identifiers.org/hco/5/GRCh38#127307108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57286048-C-A

127307108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286048-C-T

127307135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286076-A-T

127307183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286128-C-T

127307387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286309-G-A

127307393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286315-G-C

127307727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286657-C-T

127307912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286869-C-T

127308025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57286983-G-A

127308304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57287218-C-T

127308477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57287378-G-A

127309067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57287537-A-G

127309257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57287708-T-C

127309355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57287924-A-G

http://identifiers.org/hco/5/GRCh38#127309668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57288208-A-C

127309673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57288213-G-A

127309682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57288222-T-G

127309832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57288344-A-G

127309858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57288403-T-A

http://identifiers.org/hco/5/GRCh38#127310280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57289529-C-A

127310497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57289722-T-A

127310497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57289722-T-G

127310605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57289836-G-C

127310687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57289911-G-T

127310783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57290131-G-A

127311042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57290275-A-G

http://identifiers.org/hco/5/GRCh38#127311074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57290305-C-A

127311481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57290644-T-C

127311491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57290654-G-A

http://identifiers.org/hco/5/GRCh38#127311675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57290847-A-C

127311745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57290916-C-T

127311925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57291140-A-G

127312042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57291410-G-A

http://identifiers.org/hco/5/GRCh38#127312264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57291607-C-A

127312264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57291607-C-T

127312283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57291625-G-T

http://identifiers.org/hco/5/GRCh38#127312364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57291704-C-A

127312364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57291704-C-T

http://identifiers.org/hco/5/GRCh38#127312404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57291744-A-C

127312788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57292106-G-A

127312788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57292106-G-T

127313018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57292342-C-T

127313271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57292553-T-C

127313278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57292560-A-G

127313404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57292697-G-A

127313425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57292715-A-G

127313791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57293075-G-A

127313937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, undefined
orthologous variants: 57293219-T-A

127313968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57293248-A-G

127313991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, undefined
orthologous variants: 57293271-T-C

127314284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57293514-G-A

127314776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57295833-A-G

127314926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57295973-G-A

127314926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57295973-G-C

127315023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57296049-G-A

127315220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57296243-A-G

127315813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57296828-G-T

127315817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57296832-A-G

127315817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57296832-A-T

127316093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57297088-C-T

127316213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57297494-G-A

127316213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57297494-G-T

http://identifiers.org/hco/5/GRCh38#127316300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57297605-C-A

127316305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57297610-A-G

127316305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57297610-A-T

127316687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57297978-G-A

127318177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57299174-C-T

127319812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57299911-G-T

127319867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57299967-T-G

127320041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57300134-A-G

127320057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57300150-C-G

127320057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57300150-C-T

127320276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57300532-G-A

127320276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57300532-G-T

127320337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57300592-G-A

127320403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57300659-A-G

127321018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57301268-G-T

127321064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57301306-G-C

127321093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57301329-T-C

127324307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305500-A-G

127324317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305510-A-G

127324413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305600-G-A

127324640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305817-C-T

127324643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305820-G-A

127324643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305820-G-C

127324643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305820-G-T

127324682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305858-A-G

127324808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57305961-C-T

127324861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306000-C-T

127325271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306355-A-G

127325291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306375-A-G

127325469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306562-C-T

127325595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306673-C-T

127325739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306789-A-G

127325740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306790-C-T

127325756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306804-T-G

127325886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306878-T-C

127325915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306907-T-A

127325915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306907-T-G

127325919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306911-T-C

127325921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306913-T-A

127325964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57306942-C-T

127326341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57307372-A-G

http://identifiers.org/hco/5/GRCh38#127326360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57307389-A-C

127326360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57307389-A-G

127326609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57307613-A-T

127326614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57307618-G-T

127326835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57307800-G-C

127327037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308000-T-G

http://identifiers.org/hco/5/GRCh38#127327092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57308056-C-A

127327098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308062-T-C

127327283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308226-G-T

127327311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308274-T-A

127327334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308298-G-T

127327346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308310-G-A

127327396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308359-A-G

127327599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308492-G-A

127327618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308511-T-C

127327662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308549-G-C

127328101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308678-T-C

127328141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308719-T-C

127328333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308932-A-G

127328397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57308997-A-T

127328543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57309849-A-T

127328560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57309862-A-G

127328715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57310019-G-A

127328734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57310038-G-A

127328832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57310149-A-T

127328949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57310266-G-A

127328950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57310267-G-A

127329109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57310414-T-A

127329109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57310414-T-G

127329591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57311131-A-G

127329644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57311253-C-T

127329665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57311274-A-T

127329917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57311492-G-A

127330700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57312952-T-C

127330707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57312958-A-G

127330724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57312969-A-G

127330769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313016-G-C

127331113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313342-T-C

127331272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313522-G-A

127331272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313522-G-T

127331335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57313584-G-C

127331366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense variant
orthologous variants: 57313615-A-T

127331541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313748-T-C

127331542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313749-G-A

127331542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313749-G-T

127331576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313776-G-A

127331588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313788-C-G

127331654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313839-A-T

127331772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57313948-T-A

127331832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57314009-A-G

127332013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57314708-G-A

127332013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57314708-G-C

127332105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57314803-T-C

127332107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57314805-T-A

127332711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57315394-G-A

127332711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57315394-G-T

127332857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57315556-T-C

127332996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57315673-T-C

127333080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57315732-G-T

127333706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57315984-G-A

127333847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57316100-T-C

127333876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57316110-T-C

127333902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57316130-A-G

127333997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57316199-T-C

127334268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57316632-T-C

127334546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57316892-A-G

127334611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57316945-C-T

127334691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57317027-T-C

127335197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57317465-T-C

127335240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57317511-T-G

127335414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57317703-G-A

127335512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57317789-T-C

http://identifiers.org/hco/5/GRCh38#127335747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57317943-C-A

127335749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57317945-C-T

127335873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57318050-C-T

127336708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57319703-G-A

127336892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57319902-T-C

127338273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57321649-T-C

127338425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57321782-G-C

127338446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57321803-G-C

127338640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57321988-A-G

127338654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322002-T-G

127338947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322295-C-G

127339062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322506-T-G

127339092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322539-G-A

127339092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322539-G-T

127339126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57322579-A-G

127339135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57322588-G-T

127339159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57322612-T-C

127339186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57322639-T-C

127339213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57322666-G-A

127339241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322699-G-C

http://identifiers.org/hco/5/GRCh38#127339255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57322713-C-A

127339335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322797-G-A

127339335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322797-G-T

http://identifiers.org/hco/5/GRCh38#127339368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57322814-C-A

127339368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322814-C-T

127339372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322818-G-A

127339372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322818-G-T

127339442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322885-G-T

127339491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322932-G-A

127339491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57322932-G-C

127340057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57323688-T-C

127340281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57323884-T-C

127340330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57323934-G-C

127340332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57323936-G-A

127340343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57323947-A-G

http://identifiers.org/hco/5/GRCh38#127340379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57323985-C-A

127340415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324017-G-A

127340415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324017-G-T

http://identifiers.org/hco/5/GRCh38#127340428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57324030-A-C

127340428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324030-A-G

127340432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324034-G-T

127340499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324101-T-C

127340718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324346-G-A

127340862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324470-A-G

127341032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324629-G-A

127341160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324720-A-G

127341194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324750-C-G

127341246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324793-T-A

127341395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57324936-A-G

127341504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325002-G-A

127341521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325019-C-G

127341555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325052-A-G

127341610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325088-A-G

127341662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325138-A-G

127341867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325315-C-T

127341990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325437-C-T

127342293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325704-T-C

127342434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325818-A-G

127342446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325830-A-G

127342469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57325855-T-C

127342782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57326127-A-G

127342883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57326228-A-G

http://identifiers.org/hco/5/GRCh38#127342968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57326357-C-A

127342968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57326357-C-T

127343255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57326640-T-C

127344140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327090-T-A

127344142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327092-C-T

127344450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327370-G-A

127344557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327474-C-T

127344571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327484-A-G

127344630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327543-C-T

127344673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327582-A-T

127344784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327699-A-G

127344840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327753-A-T

http://identifiers.org/hco/5/GRCh38#127344976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57327859-A-C

127345113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57327986-C-T

127345133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57328006-T-C

127345345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57328222-C-G

127345369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57328247-T-C

127345378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57328256-A-G

http://identifiers.org/hco/5/GRCh38#127345481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57328354-A-C

127345579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57328447-G-A

127345625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57328490-C-T

http://identifiers.org/hco/5/GRCh38#127350677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57329427-C-A

127350677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57329427-C-T

127350725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57329474-T-G

127351219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57329558-T-G

127351251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57329578-A-T

127351385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57329713-A-G

127351633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, undefined
orthologous variants: 57330378-T-C

127351874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57330411-T-C

127351922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57330458-A-T

http://identifiers.org/hco/5/GRCh38#127352003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57330552-A-C

127352156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57330675-C-T

127352206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57330728-G-T

127352763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57330977-C-T

127352862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57331075-G-T

127352971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57331141-G-A

127353035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57331204-T-C

127353339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57331509-A-G

127353805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57331930-G-T

127353883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57332012-G-A

127353966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57332089-C-T

127354113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57332235-C-T

127354216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57332525-A-G

127354335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57332629-C-T

127355040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57333422-C-T

http://identifiers.org/hco/5/GRCh38#127355460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57333811-C-A

127355563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57333914-A-G

127355666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334015-C-T

127355767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334124-A-G

127355771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334128-A-G

127355771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334128-A-T

http://identifiers.org/hco/5/GRCh38#127356075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57334416-C-A

127356190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334525-T-C

127356220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334574-G-A

127356220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334574-G-T

127356401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57334715-A-G

http://identifiers.org/hco/5/GRCh38#127356640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57334955-A-C

127358282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57337297-T-G

127358310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, undefined
orthologous variants: 57337322-G-T

http://identifiers.org/hco/5/GRCh38#127358419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#57337425-A-C

127358464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, undefined
orthologous variants: 57337459-G-A

127359072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338028-C-T

127359265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338264-T-G

127359361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338354-G-A

127359361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338354-G-T

127359385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338373-A-G

127359433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338421-T-C

127359464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338455-C-T

http://identifiers.org/hco/5/GRCh38#127359560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57338529-C-A

127359635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338581-C-G

127359819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338850-T-A

127359869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57338891-G-A

127363147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340016-A-G

127363383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340224-T-A

127363395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340236-G-C

127363449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340292-T-G

127363500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340334-G-A

http://identifiers.org/hco/5/GRCh38#127363578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57340410-A-C

127363667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340480-A-G

127363709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340520-C-G

127363718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340529-G-A

127363860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340661-A-T

127363861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340662-C-T

127363951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57340750-A-G

127364302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57341281-A-G

http://identifiers.org/hco/5/GRCh38#127364348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57341323-A-C

127365400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57341703-G-A

127365529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57341817-C-T

127365597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57341884-G-C

127365600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57341887-C-G

127366112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57342844-G-A

127366188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57342907-G-A

127366367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57343072-T-G

127366370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57343075-T-C

127366497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57343165-T-C

127367682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57343421-A-T

127368111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57343827-G-A

127368315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57344026-C-T

127368608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57344216-G-T

127368938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57344566-C-T

127369124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57344748-T-C

127369613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345093-G-C

127369772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345252-A-G

127369825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345305-T-C

127369825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345305-T-G

127369876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345354-A-G

http://identifiers.org/hco/5/GRCh38#127369877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57345355-C-A

127369877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345355-C-T

127370013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345497-A-G

127370013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345497-A-T

127370035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345519-A-G

127370108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345591-A-G

127370121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345604-T-A

127370262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57345738-G-T

127370957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346375-T-G

127370965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346383-A-G

127371007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346431-T-A

127371055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346479-A-G

127371197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346628-G-C

127371201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346632-G-C

127371205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346636-G-C

127371247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346678-C-G

127371329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57346891-G-C

127371547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57347103-A-G

127371624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57347179-T-C

127371852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57347418-T-G

http://identifiers.org/hco/5/GRCh38#127371859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57347426-A-C

127375629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57356297-C-T

127375684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57356334-G-A

127375752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57356398-T-C

127375765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57356409-T-C

127375787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57356431-C-T

127376304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57356825-G-T

127376448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57356929-G-A

127376563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57357018-A-T

127376624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57357092-G-A

127376788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57357299-T-G

127376889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57357396-A-G

127376928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57357433-G-A

127376968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57357471-T-A

127377188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57358066-A-G

http://identifiers.org/hco/5/GRCh38#127377416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57358274-C-A

127377533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57358386-A-G

127377919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57358773-C-T

127378132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57358931-A-G

127378233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57359008-T-C

127378944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57359401-C-T

127379152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57359584-C-G

127379152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57359584-C-T

127379437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57359843-C-G

127379492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57359889-C-T

http://identifiers.org/hco/5/GRCh38#127379533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57359927-A-C

127379626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57359995-G-T

http://identifiers.org/hco/5/GRCh38#127379986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57360174-A-C

127380002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360192-G-C

127380077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360260-T-C

127380176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360403-A-G

127380185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360412-C-T

127380189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360416-C-T

127380337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360564-T-A

127380337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360564-T-C

127380982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360846-T-G

127381099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360992-G-A

127381099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57360992-G-T

127381129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57361023-A-G

127381379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57361262-T-A

127381416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57361286-C-T

127381489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57361368-G-T

127381498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57361377-G-A

127381605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57361466-G-A

127383955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57362449-G-A

http://identifiers.org/hco/5/GRCh38#127383964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57362458-C-A

127384026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57362506-T-C

http://identifiers.org/hco/5/GRCh38#127384080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57362559-C-A

127384081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57362560-C-T

127384185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57362635-C-T

127384542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57363034-G-C

127384924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57363420-C-G

127384924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57363420-C-T

127385264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57363719-A-T

http://identifiers.org/hco/5/GRCh38#127386328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57364503-C-A

127386328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57364503-C-T

127386666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57366234-A-T

http://identifiers.org/hco/5/GRCh38#127386844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57366395-A-C

127386844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57366395-A-G

127387186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57366727-A-G

127387274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57366829-C-T

127387384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57366944-A-G

127387435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57366990-T-A

127387479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57367036-A-G

127387525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57367079-G-A

127387646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57367179-G-A

http://identifiers.org/hco/5/GRCh38#127387652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57367185-C-A

127387702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57367232-T-A

127389158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57368868-G-A

127390037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369011-A-G

127390037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369011-A-T

http://identifiers.org/hco/5/GRCh38#127390162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57369140-A-C

127390184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369156-T-A

127390270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369241-G-T

127390783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369452-A-G

127390857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369513-T-G

127390971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369613-T-C

127393270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369693-G-T

127393371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369798-G-A

127393371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369798-G-C

http://identifiers.org/hco/5/GRCh38#127393457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57369880-A-C

127393501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57369912-C-T

127393734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57370154-G-C

127393754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57370174-G-A

127393754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57370174-G-T

127393798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57370220-G-A

127393987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57370407-T-C

http://identifiers.org/hco/5/GRCh38#127394069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57370498-C-A

127394069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57370498-C-T

127394291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371021-T-C

127394308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371062-G-A

127394406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371167-G-T

127394602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371349-A-G

127394622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371372-T-G

127394690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371430-C-G

127394785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371525-C-G

127394890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371630-T-A

127395047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371791-G-C

127395121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371843-T-G

127395133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371854-T-G

127395162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371888-G-A

127395188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371907-T-C

127395289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57371983-G-A

127396471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57373553-G-A

127396471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57373553-G-T

127396611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57373695-C-T

127396632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57373716-G-A

127396632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57373716-G-T

127396649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense variant
orthologous variants: 57373733-G-A

127396649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense variant
orthologous variants: 57373733-G-T

127396764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57373848-A-T

127396789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57373874-T-C

127396796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57373881-C-G

127396796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57373881-C-T

127396805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57373890-A-G

127396993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374042-A-G

127397048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374064-G-A

127397217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374228-A-G

127397264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374280-T-G

127397389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374468-C-T

127397648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374743-T-C

127397716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374814-G-T

http://identifiers.org/hco/5/GRCh38#127397828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57374918-C-A

127397828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57374918-C-T

127398620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375678-C-G

127398620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375678-C-T

127398623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375681-G-A

127398626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375684-T-C

http://identifiers.org/hco/5/GRCh38#127398627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57375685-C-A

127398627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375685-C-T

127398630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375688-G-A

127398630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375688-G-C

127398630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375688-G-T

127398706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense variant
orthologous variants: 57375765-T-A

127398806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375865-C-T

http://identifiers.org/hco/5/GRCh38#127398921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57375965-A-C

127398921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57375965-A-G

127399021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376065-A-G

127399091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376130-C-T

127399188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376224-T-C

127399476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376505-G-A

127399605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376585-C-T

127399689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376678-C-T

127399781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376771-T-C

127399901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57376820-G-A

127400494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57377524-T-C

127400590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57377626-G-C

127400779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57377797-C-G

127400842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57377848-C-T

127400965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57377967-T-G

127401010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378048-T-G

127401098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378143-G-A

127401101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378146-G-C

127401108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378154-C-G

127401228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378296-G-C

127401365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378433-C-T

127401543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378610-G-A

127401543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378610-G-T

127401752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378816-T-C

http://identifiers.org/hco/5/GRCh38#127401833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57378899-C-A

127401833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57378899-C-T

127402186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379245-G-A

127402300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379359-C-T

127402342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379401-C-T

127402396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379455-A-G

127402455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379520-C-T

127402763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379842-T-A

http://identifiers.org/hco/5/GRCh38#127402767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57379846-A-C

127402767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379846-A-G

http://identifiers.org/hco/5/GRCh38#127402812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57379891-C-A

127402812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379891-C-T

127402819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379898-G-T

127402821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379900-G-T

127402825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379904-G-A

127402825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379904-G-T

127402829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379908-G-A

127402829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57379908-G-T

127403041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57380622-G-C

127403210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381031-G-A

127403210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381031-G-T

127403248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381069-T-C

127405143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381340-A-G

127405267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381501-C-T

127405348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381565-G-A

127405502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381782-G-A

127405618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57381888-T-G

127405753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382002-T-C

127405933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382175-G-A

127406070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382281-A-G

127406198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382355-G-A

127406332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382454-A-G

127406345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382468-G-A

127406345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382468-G-C

127406500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382640-T-G

127406826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57382954-C-T

127406923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383042-A-G

127406923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383042-A-T

127407190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383285-T-G

127407202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383297-A-G

127407202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383297-A-T

127407372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383450-G-A

127407432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383500-A-G

127407504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383561-T-G

127407544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383635-A-G

127407572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57383678-A-G

127408003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57384108-T-C

127408090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57384190-C-T

127408149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57384250-T-G

127408342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57384600-C-T

127408651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57385060-G-A

127408715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57385118-A-G

127409264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57385347-G-T

127409449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57385519-A-G

127409560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57385615-C-T

127409587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57385641-C-T

http://identifiers.org/hco/5/GRCh38#127409592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57385646-C-A

http://identifiers.org/hco/5/GRCh38#127409593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57385647-C-A

127409617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57385663-G-A

127409617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57385663-G-C

127410415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57385932-C-T

127410425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57385942-T-C

http://identifiers.org/hco/5/GRCh38#127410438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57385955-A-C

127410482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57385999-C-T

127410488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57386005-C-T

127410494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57386011-T-C

127410533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57386050-G-C

127410539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57386056-T-C

127410571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57386088-G-A

127410571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57386088-G-T

127410609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57386126-T-C

127410611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57386128-A-G

127410817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57386216-G-T

127410907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57386307-T-C

http://identifiers.org/hco/5/GRCh38#127410970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57386368-C-A

127411021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57386411-A-G

127411726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57387091-T-A

127411730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57387095-G-A

127412752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57387204-T-G

127412835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57387282-A-G

127412852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57387299-C-G

127413030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57387471-G-A

127413183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57387858-T-G

127413677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57388801-C-G

127413714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57388818-A-G

127413818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57388920-C-T

127413905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389005-A-G

127414102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389164-A-G

127414257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389303-A-G

127414287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389333-C-G

127414298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389345-T-G

127414356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389401-A-T

127414400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389443-G-A

127414721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389735-T-C

127414874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389869-A-T

127416930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392045-C-T

127417299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392399-T-C

http://identifiers.org/hco/5/GRCh38#127417358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57392457-C-A

127417358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392457-C-T

127417523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392620-A-G

127417617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392714-C-T

127417627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392724-A-G

127417758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57392855-T-C

127417918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393012-T-C

http://identifiers.org/hco/5/GRCh38#127417919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57393013-C-A

127417924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393018-A-G

127417930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393024-T-C

127418018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393096-A-G

127418087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393169-T-C

127418087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393169-T-G

127418361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393419-A-G

127418505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57393566-T-G

127418950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394017-A-G

127418960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394027-T-A

127419043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394109-A-G

127419043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394109-A-T

127419158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57394221-T-C

127419236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: synonymous variant
orthologous variants: 57394299-G-A

127419236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense variant
orthologous variants: 57394299-G-T

http://identifiers.org/hco/5/GRCh38#127419318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57394373-C-A

127419318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394373-C-T

127419323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394378-G-T

127419863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394876-C-T

127419915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394929-G-A

127419915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394929-G-T

127419970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394992-G-A

127419970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394992-G-C

127419970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57394992-G-T

127420522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57395520-G-A

127420646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57395671-A-G

127420791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57395809-C-T

127420863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57395887-G-C

http://identifiers.org/hco/5/GRCh38#127421480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57396473-A-C

127421614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57396622-T-C

127422173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57397376-C-G

127422657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57397500-G-A

127422657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57397500-G-C

http://identifiers.org/hco/5/GRCh38#127422783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57397626-A-C

127422824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397667-T-A

127422825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397668-A-G

127422831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397672-G-A

127422831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397672-G-C

http://identifiers.org/hco/5/GRCh38#127422990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57397848-A-C

127422991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397849-G-A

127423452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398250-A-T

127423466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398264-T-A

127423666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398431-G-T

127423679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398443-A-G

127423681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398445-C-T

127423705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398469-G-A

127423860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398624-C-G

127423861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57398625-A-G

127424184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57399176-A-G

127424274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57399263-T-C

127424341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57399329-T-G

http://identifiers.org/hco/5/GRCh38#127424468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57399466-C-A

127424468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57399466-C-T

http://identifiers.org/hco/5/GRCh38#127424631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57399644-C-A

http://identifiers.org/hco/5/GRCh38#127424695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57399706-A-C

127424695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57399706-A-G

127424695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57399706-A-T

127424769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57399767-G-A

127424769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57399767-G-T

127424884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57399860-A-T

127425619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400642-A-T

127425641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400665-C-T

127425677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400701-A-G

127425824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400838-G-T

127426040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401040-G-T

127426220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401174-C-T

http://identifiers.org/hco/5/GRCh38#127426724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57402253-A-C

127426863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57402410-A-G

127426918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57402465-C-T

127426994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57402555-T-A

127427128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57402676-C-G

127427674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403164-T-C

127427715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403204-G-A

http://identifiers.org/hco/5/GRCh38#127427821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57403327-A-C

http://identifiers.org/hco/5/GRCh38#127427887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57403391-A-C

127427921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403425-G-A

127428135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403570-T-A

127428135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403570-T-C

127428136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403571-C-T

http://identifiers.org/hco/5/GRCh38#127428171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57403588-C-A

127428171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403588-C-G

127428171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403588-C-T

127428330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403691-G-T

127428570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403868-G-A

127428588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403884-A-G

http://identifiers.org/hco/5/GRCh38#127428631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57403925-C-A

127428743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404037-C-T

127428811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404088-C-T

127428886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404167-T-A

127428886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404167-T-C

127429074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404362-A-T

127429112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404399-C-T

127429230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404525-A-G

127429238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404533-T-G

127429347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404603-A-G

127430149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405389-G-A

127430155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405393-G-A

127430372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405582-A-G

127430689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405885-A-G

http://identifiers.org/hco/5/GRCh38#127430741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57405931-C-A

127430980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406167-G-A

127431056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406210-T-C

127431069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406223-A-G

127431267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406419-G-A

127431475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407009-C-G

127431634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407163-G-A

127431667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407192-C-G

127431734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407261-C-T

127431762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407293-G-C

127432011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407501-A-T

127432049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407541-A-G

127432196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57407660-G-T

127433085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408451-C-G

127433185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408546-G-T

127433212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408575-T-C

127433216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408579-G-T

127433345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408735-C-G

127433347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408737-A-G

127433518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408908-C-G

127433518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408908-C-T

127433526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408915-G-A

127433526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408915-G-T

127433554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408956-G-A

127433554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408956-G-T

127433561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408963-G-A

127433561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408963-G-C

127433579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408978-T-C

127433579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57408978-T-G

http://identifiers.org/hco/5/GRCh38#127433720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57409109-A-C

127433743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409133-T-C

127433780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409170-A-G

127433896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409286-G-A

127434058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409461-A-G

127434120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409527-A-G

127434212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409625-T-C

http://identifiers.org/hco/5/GRCh38#127434219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57409632-C-A

127434286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409698-G-A

127434385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409805-T-A

127434419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57409840-T-G

127434694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57410068-C-T

http://identifiers.org/hco/5/GRCh38#127434840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57410214-C-A

127434840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410214-C-T

127434859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410231-G-T

127434962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410304-G-A

127434962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410304-G-C

127434962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410304-G-T

http://identifiers.org/hco/5/GRCh38#127435211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57410531-C-A

127435211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410531-C-T

127435215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410535-T-C

127435326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410633-T-C

127435335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410642-G-A

127435407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57410714-C-T

127435631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410912-T-G

127435643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57410924-T-C

127435807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57411910-A-G

127435938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57412051-C-T

127436004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57412113-G-A

127436074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57412176-G-T

127436479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57412519-G-A

127436576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57412651-C-T

http://identifiers.org/hco/5/GRCh38#127436621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57412696-A-C

127436623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57412699-G-A

http://identifiers.org/hco/5/GRCh38#127436632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57412708-A-C

127437046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57413111-G-A

127437230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57413522-G-T

127437325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57413618-G-A

127437416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57413712-T-C

127437466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57413760-A-G

127437558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57413845-T-A

127437636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57413911-G-A

127437902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414195-T-C

127437902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414195-T-G

127437933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414225-T-G

127437977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414269-C-T

http://identifiers.org/hco/5/GRCh38#127438293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57414542-C-A

127438293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414542-C-T

http://identifiers.org/hco/5/GRCh38#127438331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57414589-C-A

127438331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414589-C-T

127438410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414664-G-A

127438414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414668-G-T

127438509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57414766-C-T

127438618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414892-G-A

127438648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57414922-G-T

127438771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415043-C-T

127438784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415056-G-A

127438862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415137-A-G

127438881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415157-G-T

127438887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415163-A-G

127438887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415163-A-T

http://identifiers.org/hco/5/GRCh38#127438925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57415201-C-A

127438932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415208-G-T

127439010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415253-G-A

127439096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415342-T-A

127439223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415475-T-C

127439303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415525-T-C

127439312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415534-C-G

127439567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415675-A-G

127439571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415679-C-G

127439634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57415744-T-C

127440070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57416170-T-C

http://identifiers.org/hco/5/GRCh38#127440619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57416750-C-A

127440619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57416750-C-T

127440637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57416770-C-T

127440654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57416787-A-T

127440716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57416843-T-A

127440761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57416888-A-G

127440773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57416900-A-G

127440774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57416901-C-T

127440794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57416921-C-T

127440898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417006-G-A

127440898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417006-G-T

127440899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417007-T-C

127440913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417011-A-G

127440931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417026-T-A

127440931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417026-T-C

127440931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417026-T-G

127440987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417077-G-A

127440987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417077-G-T

127441126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417243-T-C

127441428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417519-T-C

127441434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417525-A-T

127441502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417587-C-G

127441517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417602-C-G

127441518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417603-A-G

http://identifiers.org/hco/5/GRCh38#127441554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57417611-A-C

127441669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417724-C-T

127441808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417838-C-G

127441814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417844-C-T

127441926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417912-G-A

127441984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57417958-T-C

127442543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418451-G-A

127442577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418486-A-G

127442726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418628-T-C

127442842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418727-T-A

127442869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418753-G-T

http://identifiers.org/hco/5/GRCh38#127442885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57418769-C-A

127442885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418769-C-T

127442957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418837-T-C

127442962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418842-A-G

127442962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57418842-A-T

127443038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense variant
orthologous variants: 57418920-A-G

127443156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419040-T-G

http://identifiers.org/hco/5/GRCh38#127443215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57419089-C-A

127443215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419089-C-T

127443238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419112-T-G

127443326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419201-G-A

127443326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419201-G-T

127443373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419246-C-T

http://identifiers.org/hco/5/GRCh38#127443479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57419329-C-A

127443511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419430-G-A

127443717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57419670-T-A

127443915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57420005-G-C

127443990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron variant
orthologous variants: 57420090-T-C

http://identifiers.org/hco/5/GRCh38#127444750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57420328-C-A

127444750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57420328-C-T

127444994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57420543-T-G

127445248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57420645-G-A

127445248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57420645-G-T

http://identifiers.org/hco/5/GRCh38#127445271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57420659-C-A

127445271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57420659-C-G

127445271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57420659-C-T

127445274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57420662-G-A

http://identifiers.org/hco/5/GRCh38#127445332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57420715-C-A

127445342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57420725-G-A

127445342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57420725-G-T

127445368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57420751-A-G

127445384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57420780-G-A

127445437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57420832-A-G

http://identifiers.org/hco/5/GRCh38#127445440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57420835-C-A

127445440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57420835-C-T

127445442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57420837-C-T

127445506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57420904-T-A

127445506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57420904-T-C

127445725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57421139-T-C

127445763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57421163-G-A

127445764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57421164-G-A

127445764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57421164-G-T

http://identifiers.org/hco/5/GRCh38#127445773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57421173-C-A

127445773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57421173-C-T

127446102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57421762-G-T

http://identifiers.org/hco/5/GRCh38#127446104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57421764-C-A

127446355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422026-G-T

127446405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422077-T-C

http://identifiers.org/hco/5/GRCh38#127447660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57422458-C-A

127447660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57422458-C-T

127447698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422495-G-A

127447698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422495-G-T

127447705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422502-T-C

127447743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422538-C-T

127447818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422593-C-G

127447818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422593-C-T

127447826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422601-T-C

127447948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422691-C-T

127448051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422786-C-T

127448077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57422798-G-A

http://identifiers.org/hco/5/GRCh38#127448808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57423210-C-A

127448808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423210-C-T

127448976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423352-A-G

127449007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423383-T-C

127449007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423383-T-G

http://identifiers.org/hco/5/GRCh38#127449013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57423389-C-A

127449013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423389-C-G

127449013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423389-C-T

http://identifiers.org/hco/5/GRCh38#127449291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57423646-C-A

127449291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423646-C-T

127449314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57423669-T-G

http://identifiers.org/hco/5/GRCh38#127453053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57424265-C-A

127454254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424582-G-T

127454350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424653-G-A

127454431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424721-G-T

127454474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424763-T-C

127454474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424763-T-G

http://identifiers.org/hco/5/GRCh38#127454482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57424769-C-A

127454482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424769-C-T

127454632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424909-G-A

127454632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424909-G-T

http://identifiers.org/hco/5/GRCh38#127454672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57424921-C-A

127454705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424961-G-A

127454705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424961-G-T

127454719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424973-T-C

127454719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424973-T-G

127454723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57424977-T-C

127454768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57425021-A-G

127454880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57425118-T-C

http://identifiers.org/hco/5/GRCh38#127454990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57425211-C-A

127455297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57425521-A-G

127455387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57425627-A-T

http://identifiers.org/hco/5/GRCh38#127455442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57425682-C-A

127455447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57425687-C-T

127455465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 57425705-T-G

127455896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57425915-C-T

127456087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57426049-A-G

127456446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57426362-T-G

127456569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57426434-T-C

127456952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57426734-A-G

http://identifiers.org/hco/5/GRCh38#127457091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57426875-C-A

127457091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57426875-C-T

127457174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57426962-T-C

127457174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57426962-T-G

127457290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57427099-G-T

127457299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57427108-G-A

127457544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57427338-T-C

127457544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57427338-T-G

127457698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57427478-G-T

127457944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57427690-T-C

127457944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57427690-T-G

127458065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57427799-G-T

127458530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428246-A-G

127458531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428247-T-G

127458692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428396-A-T

127458748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428456-G-T

127458970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428662-A-T

127458996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428688-T-A

127458996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428688-T-C

http://identifiers.org/hco/5/GRCh38#127459139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57428818-C-A

127459179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428858-G-C

http://identifiers.org/hco/5/GRCh38#127459274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57428958-C-A

127459274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428958-C-T

127459339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57428973-G-T

127459384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429017-A-G

127459416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429043-G-A

127459416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429043-G-T

127459424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429051-T-C

127459611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429248-T-C

127459629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429266-G-T

http://identifiers.org/hco/5/GRCh38#127459682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57429325-C-A

127459715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429366-A-T

127459757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429402-T-C

127460173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429598-T-C

127460483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57429875-C-G

http://identifiers.org/hco/5/GRCh38#127460801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57430167-A-C

127460883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57430235-G-T

http://identifiers.org/hco/5/GRCh38#127461031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57430349-C-A

127461067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57430385-G-A

127461067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57430385-G-T

127461220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57430536-A-G

127461745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57431646-C-T

127461844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57431729-A-G

127461954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57431844-A-G

127462008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57431902-A-G

127462016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57431910-T-G

127462065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57431963-T-C

127462249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57436696-G-A

127462249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57436696-G-T

127462310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57436777-A-G

127462311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57436778-G-A

127462324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57436791-G-T

127462340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57436808-G-C

127465107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57437794-T-C

127465160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57437840-G-T

127465279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57437930-A-G

127465455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438076-T-C

127465463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438085-T-C

127465464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438086-G-C

127465464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438086-G-T

http://identifiers.org/hco/5/GRCh38#127465480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57438102-C-A

127465480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438102-C-T

127465533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438155-G-A

127465533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438155-G-T

127465539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57438160-G-A

127465633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non coding transcript exon variant
orthologous variants: 57438254-A-G

127465633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non coding transcript exon variant
orthologous variants: 57438254-A-T

127465666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non coding transcript exon variant
orthologous variants: 57438279-G-A

127465678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non coding transcript exon variant
orthologous variants: 57438288-C-T

127465705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29634
most severe consequence: non coding transcript exon variant
orthologous variants: 57438313-T-C