74408632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796124-T-A

74408647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796139-T-C

http://identifiers.org/hco/16/GRCh38#74408691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111796190-C-A

74408691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796190-C-T

http://identifiers.org/hco/16/GRCh38#74408771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111796270-C-A

74408771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796270-C-G

http://identifiers.org/hco/16/GRCh38#74408879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111796396-C-A

74408879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796396-C-T

74408895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796412-T-C

74408895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796412-T-G

74408978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796495-G-A

74408981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796498-G-A

74408981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796498-G-T

74408999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3 prime UTR variant
orthologous variants: 111796516-T-G

74409010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: missense variant
orthologous variants: 111796526-G-A

http://identifiers.org/hco/16/GRCh38#74409104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111796603-C-A

74409176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111796662-T-C

74409249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111796746-G-A

http://identifiers.org/hco/16/GRCh38#74409378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111797154-C-A

74409378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797154-C-T

74409436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797203-G-A

74409436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797203-G-C

74409436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797203-G-T

74409452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797219-T-C

74409453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797220-C-G

http://identifiers.org/hco/16/GRCh38#74409501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111797268-A-C

74409501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797268-A-T

http://identifiers.org/hco/16/GRCh38#74409502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111797269-C-A

74409502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797269-C-T

74409515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797282-G-A

74409515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797282-G-C

74409533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797300-C-T

http://identifiers.org/hco/16/GRCh38#74409540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111797307-A-C

74409540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797307-A-G

74409659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797430-G-A

74409659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797430-G-T

74409660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797431-T-C

74409713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797491-C-T

74409768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797532-G-A

74409768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797532-G-T

74409785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797546-T-A

74409855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant
orthologous variants: 111797619-A-G

74409978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797698-C-T

74410005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797726-G-A

74410005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797726-G-C

74410005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797726-G-T

74410018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797739-G-A

74410018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797739-G-C

74410036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797757-C-T

74410099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797837-C-G

74410099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797837-C-T

74410105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797843-C-T

74410185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797918-T-A

74410219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797942-C-T

74410230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111797953-C-T

74410458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798136-G-C

74410467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798152-A-G

74410519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798204-A-G

74410521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798206-G-A

74410521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798206-G-T

74410589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 3_prime_UTR_variant, missense_variant, synonymous_variant
orthologous variants: 111798274-T-C

74410643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798328-G-A

74410643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798328-G-C

74410656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798344-G-A

74410656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798344-G-C

74410656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798344-G-T

74410686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798375-C-G

74410770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 111798485-T-C

74410809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, stop_gained
orthologous variants: 111798524-C-T

74410854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798572-G-A

74410892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798605-G-A

74410948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, stop_gained, synonymous_variant
orthologous variants: 111798661-G-A

74411026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 111798739-G-A

74411026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 111798739-G-C

74411026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 111798739-G-T

74411038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 111798751-T-A

74411038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 111798751-T-C

74411082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798805-C-G

74411082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798805-C-T

74411141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798860-G-A

74411141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798860-G-C

74411141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798860-G-T

74411163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798881-A-G

74411202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798911-G-A

http://identifiers.org/hco/16/GRCh38#74411219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111798926-C-A

74411219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798926-C-G

74411219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798926-C-T

74411230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798937-G-A

74411230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111798937-G-T

74411293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111799000-G-A

74411293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111799000-G-C

74411293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111799000-G-T

74411358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799047-T-A

74411358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799047-T-C

74411453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799073-T-C

74411480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799100-T-C

74411531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799147-C-G

http://identifiers.org/hco/16/GRCh38#74411598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111799215-C-A

74411598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799215-C-G

74411598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799215-C-T

74411609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111799226-G-T

74411759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111799344-G-A

74411759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111799344-G-C

74411766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111799351-T-C

74411766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111799351-T-G

74411767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111799352-G-T

74411775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 111799360-G-A

74411775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 111799360-G-C

74411775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 111799360-G-T

74411799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799391-G-A

74411799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799391-G-C

74411799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799391-G-T

74411803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799395-G-A

74411803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799395-G-T

74411813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799405-G-A

74411813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799405-G-C

74411813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799405-G-T

http://identifiers.org/hco/16/GRCh38#74411817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111799409-C-A

http://identifiers.org/hco/16/GRCh38#74411818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111799410-C-A

74411818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799410-C-T

74411858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799446-G-A

74411858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111799446-G-T

74411926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111799514-A-G

74411988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800115-T-C

74411988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800115-T-G

74411997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800124-G-A

74411997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800124-G-T

74412049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800175-T-C

http://identifiers.org/hco/16/GRCh38#74412069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111800200-A-C

74412077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800205-C-T

http://identifiers.org/hco/16/GRCh38#74412376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111800470-A-C

74412390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800486-T-A

74412390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800486-T-C

74412390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800486-T-G

74412428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800524-G-A

74412428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111800524-G-T

74412646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801592-G-A

74412646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801592-G-T

74412671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801609-C-G

74412671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801609-C-T

http://identifiers.org/hco/16/GRCh38#74412679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111801617-A-C

http://identifiers.org/hco/16/GRCh38#74412689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111801627-C-A

74412689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801627-C-T

74412802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111801809-G-A

74412861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111801868-A-G

74412905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801912-G-C

74412950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801945-T-C

74412950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801945-T-G

74412985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801979-G-A

74412985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801979-G-C

http://identifiers.org/hco/16/GRCh38#74413002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111801994-C-A

74413002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801994-C-G

74413002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111801994-C-T

74413176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802183-C-T

http://identifiers.org/hco/16/GRCh38#74413277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111802330-C-A

74413277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802330-C-G

74413277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802330-C-T

74413283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802336-G-T

74413300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802353-G-T

74413302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802355-T-C

74413302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802355-T-G

74413351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802393-C-T

http://identifiers.org/hco/16/GRCh38#74413357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111802397-C-A

74413365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802406-A-G

74413367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802408-T-C

74413474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802506-C-T

74413481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802513-G-T

74413528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802565-C-T

http://identifiers.org/hco/16/GRCh38#74413549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111802598-C-A

74413549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802598-C-T

http://identifiers.org/hco/16/GRCh38#74413715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111802802-C-A

74413715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802802-C-G

74413715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802802-C-T

74413725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802812-G-A

http://identifiers.org/hco/16/GRCh38#74413822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111802942-A-C

74413822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111802942-A-G

74416893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111805245-G-A

74416918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111805270-T-C

74418038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111805359-C-T

74418045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111805366-T-C

74418049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111805370-G-A

74418089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111805410-A-G

http://identifiers.org/hco/16/GRCh38#74418152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111805473-A-C

74418152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111805473-A-G

74418200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111805521-T-C

74419550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111806631-C-T

74419623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111806695-G-A

74419767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111806809-G-A

74419891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111806947-C-T

74419894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111806950-T-C

74419894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111806950-T-G

74420046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807066-G-A

74420093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807096-G-A

74420093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807096-G-T

74420118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807121-C-T

74420235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807243-G-C

74420308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807322-G-A

http://identifiers.org/hco/16/GRCh38#74420624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111807600-A-C

74420796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807794-T-G

74420820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807820-G-C

74420823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807823-G-A

74420895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807890-C-T

74420913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807909-C-T

74420914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807910-G-A

74420914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807910-G-C

74420955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807945-C-G

74420962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111807952-C-T

74421042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111808030-G-A

74421053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111808041-A-G

http://identifiers.org/hco/16/GRCh38#74421092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111808081-C-A

74421092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111808081-C-T

http://identifiers.org/hco/16/GRCh38#74421132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111808119-C-A

74421138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111808126-G-A

74421180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111808165-G-A

74421180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111808165-G-C

74421187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111808172-C-T

74421201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111808186-T-C

74421201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111808186-T-G

74421243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111808245-G-A

http://identifiers.org/hco/16/GRCh38#74421289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111808283-A-C

74421290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111808284-G-A

74421321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111808315-C-G

74421321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111808315-C-T

74421348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111808342-T-C

http://identifiers.org/hco/16/GRCh38#74421362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111808355-A-C

74421382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 111808375-G-A

http://identifiers.org/hco/16/GRCh38#74421435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111808403-C-A

74421435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111808403-C-G

74421435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111808403-C-T

74421467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111808441-G-A

74421467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111808441-G-T

http://identifiers.org/hco/16/GRCh38#74421480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#111808454-C-A

74421524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111808507-C-T

74421829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111808820-C-T

74421910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33849
most severe consequence: intron variant
orthologous variants: 111808904-C-T