88715486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123208606-G-A

88715486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123208606-G-T

http://identifiers.org/hco/16/GRCh38#88715543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123208659-C-A

88715543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123208659-C-T

88715598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123208712-G-A

88715598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 123208712-G-T

88715650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123208766-G-A

88715707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123208823-C-G

88715859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123208976-G-A

88715859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123208976-G-T

http://identifiers.org/hco/16/GRCh38#88715876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123208995-C-A

88715876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123208995-C-T

88716046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123209162-G-A

88716046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123209162-G-C

88716046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123209162-G-T

88716176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123209327-C-T

88716186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123209337-G-A

88716186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123209337-G-T

http://identifiers.org/hco/16/GRCh38#88716195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123209381-C-A

88716195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123209381-C-T

http://identifiers.org/hco/16/GRCh38#88716315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#123209512-C-A

88716315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 123209512-C-G

http://identifiers.org/hco/16/GRCh38#88716349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123209596-C-A

88716349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123209596-C-T

88716456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123209703-C-G

88716456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123209703-C-T

88716639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123209876-G-A

88716763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210012-G-A

88716763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210012-G-C

88716763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210012-G-T

http://identifiers.org/hco/16/GRCh38#88716830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123210082-C-A

88716830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210082-C-G

http://identifiers.org/hco/16/GRCh38#88716839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#123210091-A-C

88716839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210091-A-G

88716857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210109-G-A

88716991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123210199-G-T

88717062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210264-G-A

88717062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210264-G-T

88717173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210375-G-A

88717173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123210375-G-C

88717173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210375-G-T

88717236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210436-A-G

88717236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210436-A-T

http://identifiers.org/hco/16/GRCh38#88717237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123210437-C-A

88717237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210437-C-G

88717237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210437-C-T

88717243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210443-G-T

http://identifiers.org/hco/16/GRCh38#88719655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123211549-C-A

88719655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123211549-C-G

88719655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123211549-C-T

http://identifiers.org/hco/16/GRCh38#88719664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123211558-C-A

88719664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123211558-C-G

88719664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123211558-C-T

http://identifiers.org/hco/16/GRCh38#88719942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123211841-C-A

88719942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123211841-C-G

88719942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123211841-C-T

http://identifiers.org/hco/16/GRCh38#88720056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123211972-C-A

88720056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123211972-C-G

88720056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123211972-C-T

88720179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123212106-G-A

88720308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123212233-G-A

88720308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123212233-G-C

88720506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123212450-C-T

http://identifiers.org/hco/16/GRCh38#88720636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123212583-C-A

88720819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123212756-T-C

http://identifiers.org/hco/16/GRCh38#88720820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123212757-A-C

88720910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123212835-G-C

88720966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123212888-G-A

88721046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123212941-C-T

88721057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123212949-G-C

88721057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123212949-G-T

88721064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123212956-C-T

88721167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 123213047-G-A

88721167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 123213047-G-C

88721167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 123213047-G-T

http://identifiers.org/hco/16/GRCh38#88721207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123213087-C-A

88721207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213087-C-G

88721207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213087-C-T

http://identifiers.org/hco/16/GRCh38#88721243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123213120-C-A

88721243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213120-C-G

88721243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213120-C-T

88721290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213167-G-A

http://identifiers.org/hco/16/GRCh38#88721329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123213206-C-A

88721329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213206-C-G

88721329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213206-C-T

88721428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 123213356-G-A

88721428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 123213356-G-C

88721428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: splice_region_variant, stop_gained
orthologous variants: 123213356-G-T

88721444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213372-G-A

88721444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213372-G-C

88721444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213372-G-T

http://identifiers.org/hco/16/GRCh38#88721470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123213414-C-A

88721470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213414-C-G

88721470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213414-C-T

88721540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 123213496-G-A

88721582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213538-G-A

88721582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213538-G-C

http://identifiers.org/hco/16/GRCh38#88721658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123213614-C-A

88721658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213614-C-G

88721658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213614-C-T

88721774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213718-G-A

88721774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213718-G-T

88721787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123213727-T-C

http://identifiers.org/hco/16/GRCh38#88721853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123213794-C-A

88721853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213794-C-G

88721853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123213794-C-T

88721942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213883-T-A

88721942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213883-T-C

88721942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213883-T-G

http://identifiers.org/hco/16/GRCh38#88722031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123213972-A-C

88722031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123213972-A-G

88722172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214150-C-T

88722193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214182-G-A

88722193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214182-G-T

88722205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214202-G-A

88722205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214202-G-T

http://identifiers.org/hco/16/GRCh38#88722223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123214219-C-A

88722223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123214219-C-G

88722223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123214219-C-T

http://identifiers.org/hco/16/GRCh38#88722241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123214237-C-A

88722241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123214237-C-G

88722241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123214237-C-T

88722407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214430-G-A

88722407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214430-G-T

http://identifiers.org/hco/16/GRCh38#88722474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123214460-A-C

88722474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123214460-A-G

http://identifiers.org/hco/16/GRCh38#88722572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123214566-C-A

88722572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123214566-C-G

88722572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123214566-C-T

88722580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123214574-T-A

88722580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123214574-T-C

88722580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123214574-T-G

88722617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123214611-T-C

http://identifiers.org/hco/16/GRCh38#88722635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123214629-C-A

88722635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123214629-C-G

88722635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123214629-C-T

88722885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123214862-G-A

88722885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123214862-G-C

88722885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123214862-G-T

88722897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123214874-G-A

88722897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123214874-G-C

88722897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123214874-G-T

88722942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123214919-T-C

88722942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123214919-T-G

88723028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215004-G-A

88723028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215004-G-C

88723028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215004-G-T

88723065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215036-C-T

http://identifiers.org/hco/16/GRCh38#88723073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123215054-C-A

88723073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215054-C-G

88723073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215054-C-T

88723075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215056-C-G

88723075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215056-C-T

http://identifiers.org/hco/16/GRCh38#88723086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123215064-C-A

88723107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123215085-C-G

88723107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123215085-C-T

88723126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123215104-C-G

88723314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123215279-T-C

88723314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123215279-T-G

88723388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215380-G-A

88723388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215380-G-T

88723398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215390-G-T

88723452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215450-T-C

88723777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215758-G-C

88723777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215758-G-T

http://identifiers.org/hco/16/GRCh38#88723788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123215768-C-A

88723851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123215821-A-G

88723864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123215831-A-T

88723901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123215868-G-A

88723901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123215868-G-T

88723913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123215880-A-G

88723967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123215934-G-T

88724982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123216267-G-A

88724982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123216267-G-T

http://identifiers.org/hco/16/GRCh38#88724997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123216282-A-C

88725016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123216301-G-A

88725016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123216301-G-T

http://identifiers.org/hco/16/GRCh38#88725040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123216325-C-A

88725040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123216325-C-G

88725040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123216325-C-T

88725146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123216413-G-A

88725146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123216413-G-C

88725146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123216413-G-T

http://identifiers.org/hco/16/GRCh38#88725274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123216572-C-A

88725274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123216572-C-G

88725274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123216572-C-T

http://identifiers.org/hco/16/GRCh38#88725445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123216831-A-C

88725445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123216831-A-G

88725445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123216831-A-T

88725446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123216832-G-A

88725446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123216832-G-C

88725446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123216832-G-T

88725615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123216998-G-A

88725615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123216998-G-C

88725615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123216998-G-T

88725636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123217019-G-A

88725636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123217019-G-C

88725636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123217019-G-T

http://identifiers.org/hco/16/GRCh38#88725720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123217104-C-A

88725720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217104-C-T

88725757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217149-G-A

88725757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217149-G-T

88725819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217223-G-A

88725819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217223-G-C

http://identifiers.org/hco/16/GRCh38#88725838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123217238-C-A

88725838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217238-C-G

88725838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217238-C-T

88725900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217281-G-A

http://identifiers.org/hco/16/GRCh38#88725921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123217290-C-A

88725921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217290-C-T

88725947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217318-C-T

http://identifiers.org/hco/16/GRCh38#88725997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123217378-C-A

88725997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217378-C-T

88726063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217409-A-G

88726063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217409-A-T

http://identifiers.org/hco/16/GRCh38#88726156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123217499-C-A

88726156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217499-C-T

88726240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217568-G-A

88726240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217568-G-C

88726240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217568-G-T

88726352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123217662-G-A

88726352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123217662-G-T

88726367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123217677-C-G

88726367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123217677-C-T

88726376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123217686-G-A

88726376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense variant
orthologous variants: 123217686-G-T

88726415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123217725-A-G

88726528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217837-C-T

88726657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217970-G-A

88726657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217970-G-C

88726657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217970-G-T

88726672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217992-G-A

88726672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217992-G-C

88726672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123217992-G-T

88726687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123218009-G-A

88726687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123218009-G-C

88726687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123218009-G-T

88726742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123218081-G-A

88726742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123218081-G-T

88726859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123218198-G-A

88726877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123218216-G-A

88726963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 123218302-C-G

88726963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 123218302-C-T

88726985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123218324-C-T

http://identifiers.org/hco/16/GRCh38#88726994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123218344-C-A

88726994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123218344-C-T

88727020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123218364-A-T

88727132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123218491-G-A

88727170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123218529-G-A

88727170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 123218529-G-T

http://identifiers.org/hco/16/GRCh38#88727550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123219339-C-A

88727550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123219339-C-G

88727550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123219339-C-T

88727621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123219410-G-A

88727621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123219410-G-C

88727621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123219410-G-T

88731164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123221153-T-A

88731164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123221153-T-C

88731164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123221153-T-G

http://identifiers.org/hco/16/GRCh38#88731200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123221184-C-A

88731200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221184-C-T

88731209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221191-T-A

88731209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221191-T-C

88731209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221191-T-G

88731223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221200-G-T

http://identifiers.org/hco/16/GRCh38#88731285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123221254-C-A

88731285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221254-C-T

http://identifiers.org/hco/16/GRCh38#88731340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123221273-C-A

88731340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221273-C-T

88731359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221284-G-A

88731359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221284-G-T

88731400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221307-G-A

88731400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221307-G-C

88731400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221307-G-T

http://identifiers.org/hco/16/GRCh38#88731403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123221311-C-A

88731403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221311-C-G

88731403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221311-C-T

88731413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123221321-G-A

88731493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221356-A-G

88731604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221451-A-T

88731616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221462-T-C

88731616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221462-T-G

88731664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221492-A-G

http://identifiers.org/hco/16/GRCh38#88731672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123221500-A-C

88731672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221500-A-T

88731734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123221557-G-A

88731782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123221605-G-A

88731782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123221605-G-C

88731842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123221665-G-A

88731881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123221704-G-A

88731881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123221704-G-C

88731881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123221704-G-T

88731919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123221742-G-A

88731919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123221742-G-T

http://identifiers.org/hco/16/GRCh38#88732004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123221805-C-A

88732004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221805-C-G

88732004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221805-C-T

88732225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222025-G-A

88732225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222025-G-C

88732225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222025-G-T

88732270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123222085-T-C

88732270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123222085-T-G

88732286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123222106-T-A

88732293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123222113-G-C

88732380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123222201-G-A

88732431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 123222252-G-A

88732431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 123222252-G-C

http://identifiers.org/hco/16/GRCh38#88732440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#123222261-A-C

88732440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 123222261-A-G

88732552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222388-T-C

88732552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222388-T-G

88732577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222434-G-A

88732577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222434-G-T

88732584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222439-C-T

88732592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222447-A-G

88733341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223205-C-T

88733380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223244-G-A

88733380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223244-G-C

88733413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223277-G-A

88733413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123223277-G-T

88733446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223310-C-G

88733446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223310-C-T

88733491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223376-G-C

88733491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223376-G-T

http://identifiers.org/hco/16/GRCh38#88733495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123223383-A-C

88733495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223383-A-G

88733600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223491-C-T

88733700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123223591-G-A

88733700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123223591-G-C

88733741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123223635-T-C

88733772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223664-G-A

88733772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223664-G-C

88733772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223664-G-T

88733881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224160-G-A

88733881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224160-G-C

88733881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224160-G-T

88733911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123224196-G-T

88734089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224334-G-T

88734144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224391-G-A

88734144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224391-G-C

88734144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224391-G-T

http://identifiers.org/hco/16/GRCh38#88734168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123224415-C-A

88734168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224415-C-G

88734168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224415-C-T

88734187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224443-G-A

88734187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224443-G-T

http://identifiers.org/hco/16/GRCh38#88734377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123224566-C-A

88734377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123224566-C-T

88734384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123224573-C-G

88734384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123224573-C-T

88734487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224676-G-A

88734487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123224676-G-T

88734502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224691-G-A

88734502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224691-G-C

88734502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224691-G-T

88734557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224747-A-G

88734557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224747-A-T

88734612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224818-T-C

88734615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224829-G-A

88734615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224829-G-C

88734632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123224868-G-A

88734655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224895-G-A

88734655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123224895-G-T

88734658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224898-G-A

88734658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224898-G-C

88734658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224898-G-T

88734730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224970-C-G

88734730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123224970-C-T

88734769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123225009-G-A

88734769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123225009-G-C

88735062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225319-C-G

88735124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225388-C-T

88735159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123225423-T-G

88735160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123225424-C-G

88735160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123225424-C-T

88735273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225534-C-T

88735285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225540-C-T

http://identifiers.org/hco/16/GRCh38#88735304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123225559-C-A

88735304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225559-C-T

88735341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225567-G-T

88735348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225574-G-A

88735671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225911-G-A

88735671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123225911-G-T

88735852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226100-G-A

88735852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226100-G-T

88735865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226111-G-C

88735888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226138-G-A

88735888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226138-G-T

88735929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226176-G-A

http://identifiers.org/hco/16/GRCh38#88736037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123226262-A-C

88736037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226262-A-G

http://identifiers.org/hco/16/GRCh38#88736061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123226282-C-A

88736061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226282-C-G

88736061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226282-C-T

http://identifiers.org/hco/16/GRCh38#88736119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123226334-C-A

88736119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226334-C-G

88736119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226334-C-T

88736132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226351-G-C

88736132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226351-G-T

88736259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123226475-G-A

88736318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123226534-C-T

88736373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123226589-G-A

88736385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123226601-G-A

88736385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123226601-G-C

88736447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226670-C-G

88736455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226678-G-A

88736455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226678-G-C

88736456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123226679-G-A

88736764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123227067-T-C

http://identifiers.org/hco/16/GRCh38#88736801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123227106-A-C

88736801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227106-A-G

http://identifiers.org/hco/16/GRCh38#88736845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123227195-C-A

88736845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227195-C-T

88736863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227208-T-A

88736863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227208-T-C

88736863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227208-T-G

88736934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227299-C-G

http://identifiers.org/hco/16/GRCh38#88737086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123227525-A-C

88737086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227525-A-G

88737095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227534-T-G

88737143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227580-G-A

88737143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227580-G-C

88737143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227580-G-T

http://identifiers.org/hco/16/GRCh38#88737177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123227613-C-A

88737177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227613-C-G

88737177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227613-C-T

88737212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 123227638-G-A

88737219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227645-T-C

88737219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227645-T-G

88737354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227754-G-C

88737354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123227754-G-T

88737633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 123227975-G-A

88737633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 123227975-G-T

88737768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123228109-G-A

88737788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123228129-C-T

http://identifiers.org/hco/16/GRCh38#88737803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#123228144-C-A

88737803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 123228144-C-G

88737803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 123228144-C-T

88737818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123228159-C-T

88737824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228165-C-G

88737832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228173-T-C

88737872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228216-G-C

88737914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123228225-C-G

88737914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123228225-C-T

http://identifiers.org/hco/16/GRCh38#88737967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123228278-C-A

88737967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123228278-C-G

88737988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123228299-C-T

88738042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123228353-G-C

http://identifiers.org/hco/16/GRCh38#88738099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123228410-C-A

88738143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228455-A-T

88738173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228475-C-T

88738259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123228537-C-T

88738349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123228627-A-G

88738349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123228627-A-T

88738411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123228689-C-T

88738462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228751-G-A

88738462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228751-G-C

88738462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228751-G-T

88738489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228787-C-T

88738496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123228794-C-G

88738508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228806-C-T

88738512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228811-G-A

88738512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228811-G-T

88738549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123228844-C-T

88738649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123228942-C-T

88738722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123229033-C-G

88738722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123229033-C-T

88738731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123229042-A-G

http://identifiers.org/hco/16/GRCh38#88738747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123229058-C-A

88738762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229071-G-A

88738762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229071-G-C

88738763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229072-G-A

88738763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229072-G-T

88738789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229096-T-A

88738789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229096-T-C

88738823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229128-G-A

88738823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229128-G-C

88738823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229128-G-T

http://identifiers.org/hco/16/GRCh38#88738860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123229174-C-A

88738860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229174-C-T

http://identifiers.org/hco/16/GRCh38#88738911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123229217-C-A

88738911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229217-C-T

88739033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229493-T-C

http://identifiers.org/hco/16/GRCh38#88739067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123229607-A-C

88739075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229615-G-A

88739075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229615-G-T

88739098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229743-G-A

88739098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229743-G-T

88739138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229786-G-A

88739138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229786-G-T

http://identifiers.org/hco/16/GRCh38#88739164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123229810-C-A

88739164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229810-C-T

http://identifiers.org/hco/16/GRCh38#88739234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123229893-C-A

88739234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229893-C-G

88739234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123229893-C-T

88739381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230045-A-G

88739381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230045-A-T

http://identifiers.org/hco/16/GRCh38#88739420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230087-C-A

88739526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230186-G-A

88739526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230186-G-T

http://identifiers.org/hco/16/GRCh38#88739527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230187-C-A

88739527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230187-C-T

http://identifiers.org/hco/16/GRCh38#88739564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230225-C-A

http://identifiers.org/hco/16/GRCh38#88739590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230251-C-A

88739713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230374-T-C

88739721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230382-C-T

88739764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230441-G-A

88739764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230441-G-T

http://identifiers.org/hco/16/GRCh38#88739787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230469-C-A

88739787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230469-C-T

http://identifiers.org/hco/16/GRCh38#88739811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230497-C-A

88739811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230497-C-G

88739811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230497-C-T

88739812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230498-A-G

88739849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230553-T-A

88739849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230553-T-C

88739920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230629-G-A

88739920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230629-G-C

http://identifiers.org/hco/16/GRCh38#88739959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230666-A-C

88740727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230766-T-A

88740727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230766-T-C

88740744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230782-G-A

88740744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230782-G-T

88740799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230820-G-A

88740799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230820-G-T

http://identifiers.org/hco/16/GRCh38#88740828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123230849-C-A

88740838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123230859-C-T

88741484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123232774-C-T

88741532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: synonymous variant
orthologous variants: 123232822-G-A

88742055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 123233007-T-A

http://identifiers.org/hco/16/GRCh38#88742136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123233098-A-C

88742136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123233098-A-G

88742244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123234289-G-A

88742244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123234289-G-T

88742282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123234337-G-A

http://identifiers.org/hco/16/GRCh38#88742284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123234346-C-A

88742284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123234346-C-T

88742489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123234529-G-A

88742489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123234529-G-T

88742492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123234532-G-A

88742492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123234532-G-C

88742492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123234532-G-T

http://identifiers.org/hco/16/GRCh38#88742514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123234551-C-A

http://identifiers.org/hco/16/GRCh38#88743165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123235469-A-C

88743165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123235469-A-G

88746234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238046-G-A

88746301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238114-T-A

88746301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238114-T-C

88746301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238114-T-G

88746403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238214-C-T

88746409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238220-G-A

http://identifiers.org/hco/16/GRCh38#88746449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123238261-C-A

88746471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238287-C-G

88746580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238393-G-T

88746901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238732-C-G

88746901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238732-C-T

88746926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123238777-G-C

88749507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123240578-C-G

88749507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123240578-C-T

http://identifiers.org/hco/16/GRCh38#88749530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123240600-C-A

88749530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123240600-C-T

http://identifiers.org/hco/16/GRCh38#88749534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123240611-C-A

88749534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123240611-C-T

88749555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123240633-G-A

88749555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123240633-G-C

88749555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123240633-G-T

88751699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123242150-C-T

88751770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123242224-C-T

88751780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123242234-C-T

88751818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123242271-T-C

88751827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123242280-C-T

88751849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123242306-G-A

88757884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247006-G-A

88757884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247006-G-C

http://identifiers.org/hco/16/GRCh38#88757972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123247093-C-A

88757972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247093-C-T

88758179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247326-A-G

88758553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247648-C-G

88758613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247725-C-T

88758645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247750-C-G

88758645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247750-C-T

88758777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123247874-T-A

88759259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123249868-C-G

88759307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123249916-C-G

88760751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123250867-G-A

88760754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123250872-G-A

88760764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123250882-C-T

88760882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251009-T-C

88760903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251032-C-T

88760989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251138-C-T

http://identifiers.org/hco/16/GRCh38#88761142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123251293-C-A

88761177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251332-G-A

88761177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251332-G-T

http://identifiers.org/hco/16/GRCh38#88761227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123251382-C-A

88761293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251448-G-C

88761318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251470-G-T

88761696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251689-A-G

88761704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251697-G-T

http://identifiers.org/hco/16/GRCh38#88761811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123251813-C-A

88761815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123251818-G-A

88762226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252155-G-A

88762226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252155-G-T

88762291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252205-G-C

88762309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252222-A-G

88762341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252254-C-T

88762600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252450-T-A

88762630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252483-C-T

http://identifiers.org/hco/16/GRCh38#88762909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123252767-C-A

88762945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252814-G-A

88762996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123252844-C-T

88763151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253006-G-A

88763151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253006-G-C

88763217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253060-C-T

88763281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253126-T-C

88763281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253126-T-G

88763792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253433-G-A

88763792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253433-G-C

88763792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123253433-G-T

88763992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123254625-T-C

88764217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123254815-G-A

88764882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123255887-T-G

http://identifiers.org/hco/16/GRCh38#88764970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123255970-C-A

88765365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123256337-G-T

88767483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257398-C-T

88767656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257568-G-A

88767668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257580-G-A

88767952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257811-T-C

88767956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257815-C-G

88767997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257868-T-A

88768045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257925-C-T

88768070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123257949-G-A

http://identifiers.org/hco/16/GRCh38#88768141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123258009-C-A

88768142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258010-C-T

88768143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258011-T-A

88768143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258011-T-G

88768564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258354-G-A

88768568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258358-C-T

88768698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258501-C-T

88768838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258629-G-C

88768899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258689-G-C

88768926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258716-G-A

88768926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258716-G-C

88768926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123258716-G-T

http://identifiers.org/hco/16/GRCh38#88768933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123258723-A-C

http://identifiers.org/hco/16/GRCh38#88768972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123258761-C-A

88773070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123263929-G-A

88773070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123263929-G-C

88773216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264039-G-A

88773398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264171-G-T

88773542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264293-G-A

88773795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264477-C-G

88773795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264477-C-T

88773869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264582-T-C

88773870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264583-T-C

88773886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264597-G-C

88773892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264603-G-A

88773893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123264604-C-G

88774140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123265258-G-A

88774148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123265272-G-C

88774628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123265558-A-G

88774742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123265678-T-C

88774848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123265765-C-G

88774852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123265771-T-C

88774892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123265802-C-T

88775220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123266089-G-A

88775220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123266089-G-C

88777624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123270227-G-T

88777784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123270406-G-A

88777784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123270406-G-T

88777803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123270423-G-C

88777815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123270435-T-C

http://identifiers.org/hco/16/GRCh38#88778278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123271093-C-A

88778396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123271211-G-A

88778566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123271384-G-C

88778656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123271489-C-T

88778689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123271532-C-G

88779581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123273695-T-A

88779637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123273752-C-T

88779641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123273758-G-T

88779738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123273862-T-C

88779814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123273906-C-G

88779814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123273906-C-T

88779860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123273960-G-A

88779944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274050-G-C

88779944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274050-G-T

88780316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274400-G-A

88780356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274433-G-A

88781154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274576-G-A

88781167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274589-G-A

88781168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123274590-T-C

88781285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123274710-C-G

88781415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274815-G-A

http://identifiers.org/hco/16/GRCh38#88781458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123274835-A-C

88781538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274901-G-A

88781538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123274901-G-C

88781758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123275117-G-A

88781945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123275288-G-A

88782470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123275485-T-G

88782587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123275588-G-T

88782680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123275670-T-G

88783100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123276039-G-C

88783311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276223-G-A

88783369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276283-A-G

88783380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276294-C-G

88783437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276349-A-G

88783511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276452-C-T

88783520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276461-T-G

88783670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276599-G-A

88783688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276614-G-A

88783715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276637-C-T

88783824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276759-G-C

88783868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276790-C-G

http://identifiers.org/hco/16/GRCh38#88783872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123276794-C-A

88783875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123276797-C-T

88784057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277014-C-G

88784057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277014-C-T

http://identifiers.org/hco/16/GRCh38#88784146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277084-C-A

88784280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277188-G-C

88784280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277188-G-T

88784301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277205-G-A

88784493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123277384-T-G

http://identifiers.org/hco/16/GRCh38#88784608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277477-C-A

88784629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123277496-G-A

http://identifiers.org/hco/16/GRCh38#88784816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277655-C-A

88784816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277655-C-G

88784816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277655-C-T

88784848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277674-G-A

88784848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277674-G-C

88784848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron variant
orthologous variants: 123277674-G-T

88784867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123277693-T-A

88784867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: intron_variant, undefined
orthologous variants: 123277693-T-C

http://identifiers.org/hco/16/GRCh38#88784982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277794-C-A

88784982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277794-C-G

88784982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277794-C-T

88785046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277853-G-A

88785046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277853-G-T

http://identifiers.org/hco/16/GRCh38#88785076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277901-C-A

88785076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277901-C-T

http://identifiers.org/hco/16/GRCh38#88785084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277909-C-A

88785084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277909-C-T

http://identifiers.org/hco/16/GRCh38#88785090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277915-C-A

88785090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277915-C-G

88785090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277915-C-T

http://identifiers.org/hco/16/GRCh38#88785103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123277932-C-A

88785103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277932-C-G

88785103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277932-C-T

88785104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277933-G-A

88785104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277933-G-C

88785104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277933-G-T

88785132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277972-G-A

88785132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: 123277972-G-T

http://identifiers.org/hco/16/GRCh38#88785161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28993
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#123278000-C-A