237486178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90841889-A-G

237486819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842447-G-A

237486819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842447-G-T

237486855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842479-C-G

237486855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842479-C-T

237486910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842521-G-A

237486910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842521-G-T

237486918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842529-G-C

237486919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842530-C-T

http://identifiers.org/hco/2/GRCh38#237487128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#90842693-C-A

237487170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron variant
orthologous variants: 90842728-C-T

237487184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron variant
orthologous variants: 90842743-G-A

237487184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron variant
orthologous variants: 90842743-G-T

237487230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, undefined
orthologous variants: 90842788-G-A

237487230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, undefined
orthologous variants: 90842788-G-C

237487230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, undefined
orthologous variants: 90842788-G-T

http://identifiers.org/hco/2/GRCh38#237487302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90842829-C-A

237487302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842829-C-T

237487400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90842902-G-A

237487400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90842902-G-T

237487406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842923-C-G

237487431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90842969-G-T

237487793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843234-T-C

237488145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843568-C-G

237488145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843568-C-T

237488342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843744-C-T

237488510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90843845-T-C

237488777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844157-G-T

237488781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844161-G-A

237488825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844203-G-C

237488843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844221-G-A

237488843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844221-G-T

237488863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844241-C-T

237488981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90844360-C-T

http://identifiers.org/hco/2/GRCh38#237489228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90844701-A-C

237489419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90844825-T-C

237489732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90845090-T-C

237490000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845331-G-A

237490000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845331-G-C

237490183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845495-G-T

237490186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90845498-C-T

237490552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90845951-A-G

237490642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90846029-A-G

http://identifiers.org/hco/2/GRCh38#237490801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90846189-A-C

237490801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90846189-A-T

http://identifiers.org/hco/2/GRCh38#237491019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90846362-C-A

237491521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847590-G-A

237491522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847591-G-A

237491523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847592-A-G

237491606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847675-A-G

237491860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90847930-C-T

237491932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848005-C-T

237492117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848166-C-T

237492683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848694-C-T

237492779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848765-C-T

237492943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90848970-C-G

237493356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849520-T-A

237493359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849523-G-A

http://identifiers.org/hco/2/GRCh38#237493379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90849543-A-C

237493379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849543-A-G

237493379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849543-A-T

237493424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90849588-G-C

237493480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90849644-C-G

237493480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90849644-C-T

237493590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849743-G-C

237493603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849754-G-T

237493703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849839-A-G

237493894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849990-A-G

237493896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90849992-T-A

237501977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90850796-G-T

237502004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90850822-G-A

237502226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90851026-A-G

237502462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851244-G-A

http://identifiers.org/hco/2/GRCh38#237502524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#90851309-C-A

237502530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851315-G-C

237502533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851318-G-A

237502557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90851342-T-A

237502719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90851493-G-A

237509968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90855104-A-G

http://identifiers.org/hco/2/GRCh38#237510049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#90855191-C-A

237510049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90855191-C-T

http://identifiers.org/hco/2/GRCh38#237510127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90855280-C-A

237510127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855280-C-G

237510127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855280-C-T

237510183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90855329-A-G

http://identifiers.org/hco/2/GRCh38#237510216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#90855360-C-A

237510255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855398-G-T

237510281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90855405-G-A

237510281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90855405-G-T

237510308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90855431-G-C

237510308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90855431-G-T

237510324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90855447-A-G

http://identifiers.org/hco/2/GRCh38#237510365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90855486-C-A

http://identifiers.org/hco/2/GRCh38#237510388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90855512-C-A

237510388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855512-C-T

237510436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855591-G-T

237510472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855609-T-C

237510489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855626-G-A

237510489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855626-G-C

237510505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855641-G-T

237510542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90855675-A-G

237510625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90855756-C-G

237510625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90855756-C-T

http://identifiers.org/hco/2/GRCh38#237510649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90855780-C-A

237510848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90855978-G-A

237510861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90855990-G-A

http://identifiers.org/hco/2/GRCh38#237511001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90856057-C-A

237511001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90856057-C-T

237511028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90856084-T-A

237511028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90856084-T-C

237511035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90856091-G-A

237511082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90856138-C-T

237518512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90857785-G-A

237518514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90857787-G-A

237518514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90857787-G-T

237518589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90857862-G-T

http://identifiers.org/hco/2/GRCh38#237518670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90857969-C-A

237518670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90857969-C-G

237518670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90857969-C-T

237518671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90857970-C-G

237518671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90857970-C-T

237518704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858021-G-A

237518704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858021-G-T

237518967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858429-G-C

237518988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858447-G-A

237519134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858521-G-A

237519173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858557-A-G

237519269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858675-T-C

237519543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858899-G-A

237519543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858899-G-C

237519543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858899-G-T

237519575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90858939-C-T

237519706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859060-C-T

237519757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859103-G-T

237519783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859127-G-A

237519783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859127-G-T

237519791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859140-A-G

237519801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859150-G-A

237519801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859150-G-T

237519824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859171-T-G

237519924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90859233-C-G

http://identifiers.org/hco/2/GRCh38#237519932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90859241-A-C

237519932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90859241-A-T

237519965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90859274-C-G

237519965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90859274-C-T

237519966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90859275-C-T

237520126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859443-C-T

http://identifiers.org/hco/2/GRCh38#237520147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90859464-C-A

237520147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859464-C-G

237520436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859912-G-C

237520436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90859912-G-T

237520602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860024-G-A

237525374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860903-C-G

237525374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860903-C-T

237525475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860979-G-A

237525475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90860979-G-C

http://identifiers.org/hco/2/GRCh38#237525571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861010-C-A

237525648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90861086-T-C

237525684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90861122-G-A

237525684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90861122-G-C

http://identifiers.org/hco/2/GRCh38#237525687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861125-C-A

237525703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90861141-G-A

237525703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90861141-G-C

237525703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90861141-G-T

http://identifiers.org/hco/2/GRCh38#237525751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861189-C-A

237525751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90861189-C-T

http://identifiers.org/hco/2/GRCh38#237525758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861196-C-A

237525758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90861196-C-T

http://identifiers.org/hco/2/GRCh38#237525822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861259-A-C

http://identifiers.org/hco/2/GRCh38#237525882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861323-C-A

237525882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861323-C-T

237525890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861331-T-C

http://identifiers.org/hco/2/GRCh38#237525894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861335-A-C

237525937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861367-T-A

237525937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861367-T-C

http://identifiers.org/hco/2/GRCh38#237525954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90861372-C-A

237525954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861372-C-T

237526100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861513-A-G

237526251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861639-G-A

237526424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861773-C-T

237526540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861870-G-T

237526544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861874-C-G

237526673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90861984-G-C

237526748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90862053-C-T

http://identifiers.org/hco/2/GRCh38#237526763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90862067-C-A

237526763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90862067-C-T

237526942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90862219-G-A

237527016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90862284-A-G

http://identifiers.org/hco/2/GRCh38#237527022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90862290-A-C

237527244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90862932-A-G

http://identifiers.org/hco/2/GRCh38#237527258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90862943-A-C

237527320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90862982-G-A

237527496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90863154-C-T

237527528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90863185-T-A

237527559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90863208-G-A

237527559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90863208-G-C

237527559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90863208-G-T

237527639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90863324-G-C

237527639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90863324-G-T

237527643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90863328-A-G

237533678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90864589-G-A

237533829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90864741-T-C

237533885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90864781-C-T

237533920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90864812-A-G

237533979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90864875-T-C

237534233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865077-G-A

http://identifiers.org/hco/2/GRCh38#237534337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90865168-A-C

237534337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865168-A-T

237534343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865174-C-T

237534422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865253-T-C

237534523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865325-C-G

237534523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865325-C-T

237534529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865331-G-A

237534560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90865372-G-T

237534625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90865437-C-G

237534625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90865437-C-T

237534642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90865454-G-A

237534713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90865518-G-A

237540301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90867026-G-T

237540333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90867066-G-C

http://identifiers.org/hco/2/GRCh38#237540617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90867286-C-A

237540617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867286-C-T

237540743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867384-T-C

237540745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867386-G-A

237540745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867386-G-T

237540819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90867459-T-A

237540819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90867459-T-C

http://identifiers.org/hco/2/GRCh38#237541010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90867653-C-A

237541010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867653-C-T

237541049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867693-C-T

http://identifiers.org/hco/2/GRCh38#237541082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90867724-C-A

237541082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867724-C-G

237541082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867724-C-T

237541175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867770-T-C

237541318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867910-G-A

237541319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867911-G-A

237541327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90867918-G-T

237541419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90868000-C-G

http://identifiers.org/hco/2/GRCh38#237541637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90868228-C-A

237541856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90868470-C-T

237541880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90868497-C-T

237541924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90868752-A-G

237542006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90868834-C-T

237542007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90868835-G-A

237542098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90868942-T-C

237542213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869132-A-G

237542213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869132-A-T

237542282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869185-C-G

237542348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869252-A-T

237542508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869340-T-C

237542508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869340-T-G

237542544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869379-T-C

237542548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90869385-G-T

237542579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90869422-G-A

237542579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90869422-G-T

237542641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90869484-G-A

237542641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90869484-G-C

237546517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90870513-T-A

237546517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90870513-T-C

237546559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90870548-G-A

237548281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90870901-C-T

237548416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871027-G-A

http://identifiers.org/hco/2/GRCh38#237549287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90871480-C-A

237549287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871480-C-T

http://identifiers.org/hco/2/GRCh38#237549304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90871500-C-A

237549304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871500-C-G

237549304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871500-C-T

237549316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871512-G-A

http://identifiers.org/hco/2/GRCh38#237549400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90871594-C-A

237549411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871605-T-G

237549477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871655-T-C

237549599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90871739-A-G

237550380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872076-C-T

237550921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872222-G-A

237550921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872222-G-T

237551136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872401-A-G

237551326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872591-A-T

237551544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872753-T-G

237551587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872795-C-T

237551625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90872830-T-C

http://identifiers.org/hco/2/GRCh38#237552089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90872952-C-A

237552089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90872952-C-T

http://identifiers.org/hco/2/GRCh38#237552229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90873239-A-C

237552229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90873239-A-G

237552241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90873251-T-C

237552294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90873302-T-A

237552294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90873302-T-C

237552339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90873338-A-G

237553417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90876057-G-A

237553417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90876057-G-T

237553453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90876124-T-A

237553453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90876124-T-C

http://identifiers.org/hco/2/GRCh38#237553457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876128-C-A

http://identifiers.org/hco/2/GRCh38#237553459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876130-C-A

237553459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90876130-C-T

237553461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90876132-T-C

http://identifiers.org/hco/2/GRCh38#237553463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876134-C-A

http://identifiers.org/hco/2/GRCh38#237553648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876395-A-C

http://identifiers.org/hco/2/GRCh38#237553757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876502-C-A

237553772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876518-T-A

237553772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876518-T-C

http://identifiers.org/hco/2/GRCh38#237553776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876522-C-A

237553776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876522-C-T

237553791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876535-A-G

http://identifiers.org/hco/2/GRCh38#237553842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876573-C-A

237553842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876573-C-G

237553888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876616-A-G

237553905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876632-A-T

http://identifiers.org/hco/2/GRCh38#237553932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876656-C-A

http://identifiers.org/hco/2/GRCh38#237553950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876674-C-A

237554020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876739-A-G

http://identifiers.org/hco/2/GRCh38#237554024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90876743-C-A

237554024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876743-C-T

237554025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876744-G-A

237554025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29643
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90876744-G-T