83535625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100993585-C-G

83535625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100993585-C-T

83535627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100993587-G-A

83535627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100993587-G-T

http://identifiers.org/hco/4/GRCh38#83535719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100993792-C-A

83535719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100993792-C-G

83535748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: missense_variant, undefined
orthologous variants: 100993817-T-C

http://identifiers.org/hco/4/GRCh38#83535787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100993859-C-A

83535787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: missense variant
orthologous variants: 100993859-C-T

http://identifiers.org/hco/4/GRCh38#83535836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100993908-C-A

83535836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: missense_variant, undefined
orthologous variants: 100993908-C-T

http://identifiers.org/hco/4/GRCh38#83535838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100993910-C-A

83535838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: missense_variant, undefined
orthologous variants: 100993910-C-T

http://identifiers.org/hco/4/GRCh38#83535864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100993938-A-C

83535864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: synonymous_variant, undefined
orthologous variants: 100993938-A-G

83535932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100993986-T-C

83535951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100994005-T-C

http://identifiers.org/hco/4/GRCh38#83535953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994007-C-A

83535953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100994007-C-T

http://identifiers.org/hco/4/GRCh38#83536021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994068-C-A

83536021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100994068-C-T

83536027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100994074-G-C

83536027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100994074-G-T

http://identifiers.org/hco/4/GRCh38#83536122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994168-C-A

83536161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994182-C-T

http://identifiers.org/hco/4/GRCh38#83536193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994214-C-A

83536193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994214-C-T

83536299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994319-G-T

83536377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994395-T-A

83536388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994405-C-T

83536395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994412-A-G

http://identifiers.org/hco/4/GRCh38#83536408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994425-A-C

83536408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994425-A-G

http://identifiers.org/hco/4/GRCh38#83536426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994438-C-A

83536426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100994438-C-T

http://identifiers.org/hco/4/GRCh38#83536460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994474-C-A

83536460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994474-C-T

http://identifiers.org/hco/4/GRCh38#83536461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994475-C-A

83536461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994475-C-G

83536461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100994475-C-T

http://identifiers.org/hco/4/GRCh38#83536468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994482-C-A

http://identifiers.org/hco/4/GRCh38#83536617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100994668-C-A

83536617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100994668-C-G

83536617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 100994668-C-T

83536643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100994694-C-T

83536685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100994736-C-T

83536770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100994821-G-T

83536782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994833-G-A

83536782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994833-G-T

83536852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994938-A-G

83536859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994945-T-C

83536894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994977-G-C

83536894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994977-G-T

83536912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994995-T-A

83536912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100994995-T-C

83537019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100995078-T-C

83537049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100995108-A-G

83537307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100995525-A-G

83537383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100995582-G-A

83537383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100995582-G-C

83537511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100995696-T-C

83537523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100995708-G-A

83538006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100996074-T-A

83538049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100996120-C-T

83538423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100996584-A-G

83538426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100996587-G-A

83538426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100996587-G-T

83540209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101001297-G-A

83540328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101001452-G-T

83540333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101001457-T-G

83540717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101001823-G-A

83540808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101001879-G-A

83540898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101001939-C-T

83540949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101002023-T-C

83540950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101002024-A-G

http://identifiers.org/hco/4/GRCh38#83541083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101002238-A-C

83541084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101002239-T-C

83541087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101002246-C-T

83541101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101002261-A-G

83541254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101002408-G-T

83541691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101002881-T-C

83541946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101003038-T-G

83542250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101003262-A-G

http://identifiers.org/hco/4/GRCh38#83542280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101003292-A-C

83542323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101003338-C-T

83544427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101004910-G-T

83544458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101004935-T-G

83544651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101005121-A-G

http://identifiers.org/hco/4/GRCh38#83544700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101005395-C-A

83544771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101005464-A-G

83546751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008464-C-G

83546771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008484-G-A

83546940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008614-G-C

83546942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008616-C-T

83547036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008709-T-C

83547080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008753-C-T

83547115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008835-G-A

83547152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101008868-G-A

83547885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101009162-C-T

83547890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101009167-T-C

83548000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101009199-G-C

83548009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101009208-C-T

83548029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101009228-A-G

83548107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101009290-T-G

83548192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101009373-C-T

83548526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, undefined
orthologous variants: 101009788-A-G

83548615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, undefined
orthologous variants: 101009894-T-C

83548704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, undefined
orthologous variants: 101009963-T-G

83548977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101010177-A-T

83552032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011160-G-A

83552178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011305-A-G

83552323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011427-T-C

83552369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011437-A-G

83552530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011573-C-G

83552534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011577-G-A

83552580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011628-T-C

83552714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011775-G-C

83552719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011782-G-T

83552739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011805-G-T

83552747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101011813-G-A

83555558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101013569-T-C

83555561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101013572-C-T

83556213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101014203-A-G

83556587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101014306-A-G

83556701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101014419-T-C

83556744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101014456-T-A

83556745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101014457-G-A

83559342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101018480-G-T

83559448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101018575-C-T

83559468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101018594-C-T

83559469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101018595-G-A

83559472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101018598-T-C

83559480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101018607-C-T

83559783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101018882-C-T

83559905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101019002-G-C

83559915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101019012-A-G

83560119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101019200-T-C

83572724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101022973-A-G

83572728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101022977-C-T

83572847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023104-T-C

83572854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023111-A-T

83572891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023147-A-G

83572922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023178-G-A

83572945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023201-A-G

http://identifiers.org/hco/4/GRCh38#83573495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101023353-C-A

83573521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023379-C-T

83573530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023388-C-T

83573593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023453-C-T

83573644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023502-T-C

83573718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023560-C-T

83573811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023675-G-A

83573868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101023725-C-T

83574415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101025023-T-C

83574431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101025039-T-C

83574714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101025274-G-T

83574808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101025359-G-A

83574881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026340-T-G

83575022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026470-G-A

83575026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026474-G-A

83575026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026474-G-C

83575037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026485-A-G

83575037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026485-A-T

83575065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026570-G-A

83575105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026628-T-A

83575108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026631-C-T

83575122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026687-C-T

83575155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026741-C-T

83575156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026742-G-A

83575317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026907-T-G

83575353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101026943-T-G

83578155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101027780-C-T

83578160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101027785-G-A

83578321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101027923-C-T

83578436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101028040-G-A

83578946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101028542-T-C

83578950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101028546-T-C

83578952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101028548-C-T

83578986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101028582-T-C

83578990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101028586-T-C

http://identifiers.org/hco/4/GRCh38#83578997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101028593-C-A

83578997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101028593-C-T

83581394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101030895-T-A

83581412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101030913-G-T

83581441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101030931-T-A

http://identifiers.org/hco/4/GRCh38#83581489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101030965-C-A

http://identifiers.org/hco/4/GRCh38#83581513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101030989-A-C

83581513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101030989-A-G

83581770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: synonymous variant
orthologous variants: 101031264-G-A

http://identifiers.org/hco/4/GRCh38#83581797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101031291-C-A

83581797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: synonymous variant
orthologous variants: 101031291-C-T

83582045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101031497-G-A

83582083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101031519-C-G

83582127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101031554-G-C

83582127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101031554-G-T

83587189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032105-G-T

83587217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032146-T-A

83587217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032146-T-G

83587240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032169-T-G

83587518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032354-C-T

83587806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032416-T-C

83588126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032745-G-A

83588138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032756-A-G

83588142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101032760-A-G

83588282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101032898-C-T

83588330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101032943-T-G

83588347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101032953-A-G

83588364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101032954-G-A

83588364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101032954-G-T

83588369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101032959-G-A

83588374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101032964-T-A

83588383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101032973-A-G

http://identifiers.org/hco/4/GRCh38#83588445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101033034-C-A

83588445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033034-C-T

83588448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033037-G-A

83588448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033037-G-T

http://identifiers.org/hco/4/GRCh38#83588461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101033045-A-C

83588564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033132-C-T

83589050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033427-A-G

83590128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033709-A-T

83590143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033724-T-C

83590143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033724-T-G

83590144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033725-T-G

http://identifiers.org/hco/4/GRCh38#83590146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101033727-C-A

83590146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033727-C-T

83590151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033732-T-C

83590260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101033853-T-C

83590274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101033867-G-A

83590328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033919-T-C

83590341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101033964-G-T

83590469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101034222-G-C

83590797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101034532-A-G

83590887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101034621-T-C

83591044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101034769-C-G

83591405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101035791-C-T

83591476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101035863-G-A

83591515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101035895-T-C

83591547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101035932-C-T

83591572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101035954-A-G

http://identifiers.org/hco/4/GRCh38#83592153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101037002-C-A

83592153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037002-C-G

http://identifiers.org/hco/4/GRCh38#83594072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101037132-C-A

http://identifiers.org/hco/4/GRCh38#83594125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101037172-C-A

83594328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037459-A-G

83594379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037510-A-G

83594487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037603-C-T

83594558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037673-T-C

83594677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037796-T-C

83594693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037814-G-C

83594693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037814-G-T

http://identifiers.org/hco/4/GRCh38#83594726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101037849-C-A

http://identifiers.org/hco/4/GRCh38#83594835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101037959-C-A

83594835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101037959-C-G

83595017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101038141-G-C

83595169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101038297-G-T

http://identifiers.org/hco/4/GRCh38#83595202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101038331-A-C

83595202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101038331-A-G

83596594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039303-C-T

83596646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039352-G-A

83596673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039379-A-G

http://identifiers.org/hco/4/GRCh38#83596733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101039409-C-A

83596733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039409-C-T

83596829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039486-C-T

http://identifiers.org/hco/4/GRCh38#83596842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101039493-C-A

83596842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039493-C-T

83596996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039612-T-C

83597036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039636-A-G

83597036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039636-A-T

83597195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039779-T-G

83597306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039935-G-A

83597307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101039936-T-C

83597362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040073-T-C

83597372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040107-T-C

http://identifiers.org/hco/4/GRCh38#83597390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101040125-C-A

83597390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040125-C-T

83597549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040277-T-C

83597549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040277-T-G

83597572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040319-T-C

http://identifiers.org/hco/4/GRCh38#83597586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101040344-C-A

83597586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040344-C-T

83597598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040356-A-G

83597603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040361-T-C

http://identifiers.org/hco/4/GRCh38#83597642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101040394-C-A

83597642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040394-C-T

http://identifiers.org/hco/4/GRCh38#83597661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101040410-C-A

83597661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040410-C-T

83597818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101040715-T-A

83598149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: synonymous variant
orthologous variants: 101041036-C-T

83598249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron variant
orthologous variants: 101041144-C-T

83598630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101041289-T-C

83598630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101041289-T-G

83598685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101041340-T-C

83598712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101041367-T-C

83602514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101043796-T-C

83602577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101043860-A-G

83603025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101044260-G-A

83603095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101044307-A-G

83603218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101044438-A-G

83603799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101044981-A-G

83603896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101045042-T-C

83603955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101045114-G-A

83604021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101045189-G-C

83604453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101045404-G-C

83604519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101045467-G-T

http://identifiers.org/hco/4/GRCh38#83604677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101045592-A-C

83604770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045685-G-T

83604819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045747-G-A

83604819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045747-G-T

83604823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045751-T-G

83604886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045815-T-A

83604893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045822-A-G

83604893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045822-A-T

http://identifiers.org/hco/4/GRCh38#83604895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101045824-C-A

83604895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101045824-C-G

83605093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101046017-G-A

83605093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101046017-G-T

83605249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3 prime UTR variant
orthologous variants: 101046348-G-A

http://identifiers.org/hco/4/GRCh38#83605386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101046479-A-C

83605442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3 prime UTR variant
orthologous variants: 101046522-C-T

83605640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3 prime UTR variant
orthologous variants: 101046729-C-T

http://identifiers.org/hco/4/GRCh38#83605739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#101046828-C-A

83605865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28157
most severe consequence: 3 prime UTR variant
orthologous variants: 101046955-A-G