105360868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43162290-T-A

http://identifiers.org/hco/2/GRCh38#105361074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43162487-C-A

105361173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43162571-G-C

105361173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43162571-G-T

105361531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43162937-G-C

105361531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43162937-G-T

105361547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43162953-T-C

105361564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43162974-G-T

105361613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43163022-G-C

105362228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43166147-G-A

105362248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43166167-G-A

105362556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43166801-A-G

105362893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167103-G-T

105363058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167206-G-A

105363058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167206-G-C

105363058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167206-G-T

105363065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167212-T-C

105363065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167212-T-G

105363098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167245-T-C

105363129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167258-A-G

105363129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167258-A-T

105363135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167264-A-G

105363135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167264-A-T

105363218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167325-G-A

105363218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43167325-G-T

105363444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 43167563-G-A

105363444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 43167563-G-T

105363489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43167609-A-G

105363545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43167662-G-A

105363545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43167662-G-T

http://identifiers.org/hco/2/GRCh38#105363577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43167702-A-C

105363743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168264-G-A

105363748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168269-C-G

105363776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168296-G-A

105364090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168484-C-G

http://identifiers.org/hco/2/GRCh38#105364380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43168545-C-A

105364383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168548-G-A

105364575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168689-T-A

105364817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168903-A-G

105364818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168904-G-T

105364851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43168927-G-A

105364993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43169059-A-G

105365089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43169162-A-G

105367222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170523-T-C

105367224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170525-T-A

105367224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170525-T-C

105367234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170536-A-T

105367253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170556-A-G

105367424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170693-G-T

105367432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170694-T-C

http://identifiers.org/hco/2/GRCh38#105367457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43170719-C-A

105367457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170719-C-T

105367458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43170720-A-T

105367563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 43170805-G-A

http://identifiers.org/hco/2/GRCh38#105367702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43170944-A-C

105367768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171009-A-G

http://identifiers.org/hco/2/GRCh38#105367839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43171082-C-A

http://identifiers.org/hco/2/GRCh38#105367845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43171088-C-A

105367846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171089-A-G

http://identifiers.org/hco/2/GRCh38#105367858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43171101-C-A

105367858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171101-C-G

105367858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171101-C-T

105367867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171110-G-A

105367867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171110-G-C

105367867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171110-G-T

http://identifiers.org/hco/2/GRCh38#105367879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43171122-A-C

105367879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171122-A-G

105367966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43171189-A-G

105368200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43172452-C-T

105369492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43173601-G-A

105372106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43176570-G-T

http://identifiers.org/hco/2/GRCh38#105372881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43179790-A-C

105372881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43179790-A-G

105372984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43179904-A-G

105373076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180029-T-C

105373265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180195-G-A

http://identifiers.org/hco/2/GRCh38#105373434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43180735-C-A

http://identifiers.org/hco/2/GRCh38#105373440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43180741-C-A

105373441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180742-A-G

105373461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180764-G-T

105373505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180794-G-A

105373505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180794-G-T

105373519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180808-G-A

105373533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43180832-C-T

105373551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 43180850-C-T

105373596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 43180895-T-G

105373689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 43180988-G-A

105373781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181089-T-C

http://identifiers.org/hco/2/GRCh38#105375681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43181511-C-A

105375681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181511-C-T

105375708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181537-A-G

105375878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181692-T-C

105375914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181737-T-A

105375972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181795-C-T

105376043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181895-T-C

http://identifiers.org/hco/2/GRCh38#105376067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43181919-C-A

105376067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43181919-C-T

http://identifiers.org/hco/2/GRCh38#105376095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43182006-C-A

105376095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182006-C-T

105376114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182025-T-C

http://identifiers.org/hco/2/GRCh38#105376186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43182093-C-A

http://identifiers.org/hco/2/GRCh38#105377709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43182218-C-A

105377709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182218-C-T

http://identifiers.org/hco/2/GRCh38#105377710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43182219-C-A

105377710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 43182219-C-G

105377712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 43182221-G-T

http://identifiers.org/hco/2/GRCh38#105377729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43182238-C-A

105377729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182238-C-T

105377744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182252-G-A

105377766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182274-G-A

http://identifiers.org/hco/2/GRCh38#105377777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43182285-C-A

105377777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182285-C-T

105377782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182286-G-T

105377783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182287-A-G

105377784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182288-G-A

105377801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182299-A-T

105377816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182311-G-A

105377816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182311-G-C

105377816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182311-G-T

105377878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43182351-T-C

105378111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_lost, undefined
orthologous variants: 43182616-A-G

105378769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183497-A-G

105378822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183550-T-A

105378843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183570-C-T

105378861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183588-G-T

105378899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183653-G-A

105378899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183653-G-T

105378902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183656-G-A

105378902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183656-G-T

http://identifiers.org/hco/2/GRCh38#105378939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43183693-C-A

105379173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183893-C-G

105379173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183893-C-T

105379175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183895-C-G

105379217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183938-C-T

105379241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43183980-A-G

105379893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43184736-C-T

105380058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43184865-C-G

105380058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43184865-C-T

105380663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43185561-C-T

105380902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43185858-C-T

http://identifiers.org/hco/2/GRCh38#105381147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43186091-A-C

105381235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43186178-T-G

105381423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43186370-T-C

105381560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43186508-C-T

105381637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43186542-C-T

105382417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43188420-G-A

105382440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43188430-C-G

105382440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43188430-C-T

105383221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43188848-C-T

105383242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43188869-A-G

105383285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43188912-A-G

105383738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43189361-G-A

http://identifiers.org/hco/2/GRCh38#105383755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43189373-C-A

105383755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43189373-C-T

105383902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43189517-C-T

105384238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43189857-A-G

105384256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43189877-C-T

105384856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43190470-G-A

105384904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43190526-G-A

105384997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43190652-A-G

105385509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43191151-C-T

105385516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43191158-C-G

http://identifiers.org/hco/2/GRCh38#105385795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43191692-C-A

http://identifiers.org/hco/2/GRCh38#105385868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43191761-C-A

http://identifiers.org/hco/2/GRCh38#105385906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43191798-C-A

105385934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43191827-A-G

105385934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43191827-A-T

105386076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43191964-G-A

http://identifiers.org/hco/2/GRCh38#105386161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43192045-C-A

105386161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192045-C-T

http://identifiers.org/hco/2/GRCh38#105386162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43192046-C-A

105386162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192046-C-T

105386218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192092-A-G

105386252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192125-G-A

105386252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192125-G-T

105386253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192126-G-A

105386253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192126-G-T

105386317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43192185-T-G

105386508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 43192383-C-T

105386582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43192466-T-A

http://identifiers.org/hco/2/GRCh38#105386637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43192498-C-A

105386637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43192498-C-G

105386637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43192498-C-T

105387379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43192858-C-G

105388340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43193191-G-C

105388397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43193253-G-C

105388957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43193497-C-T

105389206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43193742-T-C

105389703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43194206-C-G

105389794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43194298-G-T

105389856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43194345-T-G

105389923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43194398-A-G

105391482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

105391662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

105391670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

http://identifiers.org/hco/2/GRCh38#105391815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43196912-A-C

105391850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43196947-C-G

105392057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43197150-C-T

http://identifiers.org/hco/2/GRCh38#105392158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43197231-C-A

105392158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43197231-C-T

http://identifiers.org/hco/2/GRCh38#105392551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43197288-A-C

105392551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43197288-A-G

http://identifiers.org/hco/2/GRCh38#105393021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43197559-C-A

105393086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43197637-G-A

105393096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43197647-G-C

105393101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43197652-C-T

105393660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43198341-G-T

105394905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43199320-G-A

105395197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43199603-T-C

105395210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43199616-A-G

105395217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43199623-C-G

105395217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43199623-C-T

105395685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43200031-C-T

http://identifiers.org/hco/2/GRCh38#105396968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43200945-C-A

http://identifiers.org/hco/2/GRCh38#105396975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43200952-C-A

105396975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43200952-C-T

105397002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43201004-T-A

105397002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43201004-T-C

105397002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43201004-T-G

105397027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43201030-T-A

105397027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43201030-T-G

http://identifiers.org/hco/2/GRCh38#105397038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43201082-A-C

105397038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43201082-A-T

105397119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43201158-T-C

105397262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43201267-C-T

105397349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43201347-A-G

105397510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43201414-G-A

105397548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43201448-C-T

105398078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202023-T-C

105398330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202230-T-C

105398335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202235-G-A

105398515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202409-G-A

105398531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202420-A-T

105398569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43202455-C-T

105398684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43202589-C-T

105398694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43202599-G-C

105398694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43202599-G-T

http://identifiers.org/hco/2/GRCh38#105398709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43202657-A-C

http://identifiers.org/hco/2/GRCh38#105398711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43202669-C-A

105398711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202669-C-T

105398737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202721-G-A

105398737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202721-G-C

105398737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202721-G-T

105398803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202799-A-G

105398803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43202799-A-T

105398897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43202906-G-A

105398897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43202906-G-C

http://identifiers.org/hco/2/GRCh38#105398899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#43202908-C-A

105398910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43202919-A-G

105398924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43202933-A-G

105399081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203123-A-G

105399117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203159-A-G

105399138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203192-G-A

105399138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203192-G-C

105399138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203192-G-T

105399437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43203484-G-A

105399479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203541-A-G

105399495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43203555-C-T

105399537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203599-G-A

105399587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43203652-T-C

105399629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203687-G-A

105399650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43203707-G-A

105399728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43203783-G-T

105399733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43203788-G-T

105400086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43204449-G-T

105400196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43204543-G-A

105400508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43204826-G-T

105400538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43204847-T-G

105400626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43204934-A-G

105400703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43205013-A-T

105400704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43205014-G-C

105400704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43205014-G-T

105400817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43205287-T-A

http://identifiers.org/hco/2/GRCh38#105400840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43205308-A-C

http://identifiers.org/hco/2/GRCh38#105400996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43205445-A-C

http://identifiers.org/hco/2/GRCh38#105401424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43205826-A-C

105401510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43205910-C-G

105401642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206039-C-T

105401668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206065-G-C

105401764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206159-T-C

105401840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206235-G-A

105401852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206246-T-A

105401898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206288-A-G

105402563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206395-T-A

105402563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206395-T-C

105402741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43206560-T-G

105403234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43207018-A-G

105403264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43207057-A-G

105403266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43207059-A-G

105403707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43207407-G-A

105403918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43207595-T-C

105403969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43207648-C-G

105403969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43207648-C-T

105403999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43207671-G-A

105404089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43207758-A-T

105404391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208066-C-T

105404682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208311-T-C

105404743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208365-C-G

105404928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208544-G-A

105404928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208544-G-C

105405115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208752-G-A

105405130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208767-C-T

105405152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43208793-C-T

105405548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209252-A-G

105405926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209666-A-T

105406003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209750-T-A

105406030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209767-C-G

105406060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209800-G-A

105406112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209854-A-G

105406113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209855-T-C

105406175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209912-G-C

105406254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43209992-C-G

105406300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43210049-C-G

105406300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43210049-C-T

105406421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43210170-G-C

105406484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43210220-T-C

105406502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43210234-C-T

http://identifiers.org/hco/2/GRCh38#105406511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43210243-A-C

105406595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43210311-G-A

105406754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43210464-T-A

http://identifiers.org/hco/2/GRCh38#105407534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43211182-A-C

105407591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211243-C-T

105407598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211250-C-G

105407679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211333-G-C

105407707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211362-C-G

105407707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211362-C-T

105407708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211363-A-G

105407810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211430-C-T

http://identifiers.org/hco/2/GRCh38#105407874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43211489-A-C

105407874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211489-A-T

105407936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211546-A-G

105407969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211580-A-G

105407994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211606-A-G

105408066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211667-T-A

105408220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43211833-A-G

105409941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43212581-T-C

105409977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron_variant, undefined
orthologous variants: 43212616-A-G

105410193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43212764-C-G

105410245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43212807-C-T

105410268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43212830-G-C

105410310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43212873-G-T

105410557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213085-T-A

105410659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213187-G-A

105410682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213210-G-A

http://identifiers.org/hco/2/GRCh38#105410883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43213416-A-C

105410883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213416-A-G

http://identifiers.org/hco/2/GRCh38#105410931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43213479-A-C

105410931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213479-A-T

http://identifiers.org/hco/2/GRCh38#105411135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43213666-C-A

105411247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213738-G-T

105411288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213768-T-A

105411288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213768-T-C

105411411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213886-T-C

105411424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213899-A-G

http://identifiers.org/hco/2/GRCh38#105411437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43213912-C-A

105411463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213937-T-C

105411510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213986-T-A

105411510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213986-T-G

105411517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43213993-G-T

http://identifiers.org/hco/2/GRCh38#105411532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43214009-C-A

105411532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43214009-C-T

105411844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43214142-C-T

105412206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43214427-T-C

105415499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -C-G

105415587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -C-T

105415604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -A-G

105415643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -T-G

105415867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -A-G

105416052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -C-T

105419098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43218024-A-G

105419108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43218034-G-A

105419492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43218231-C-G

105420008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43218653-T-C

http://identifiers.org/hco/2/GRCh38#105420073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43218713-C-A

105420073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43218713-C-T

105420202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43218822-G-C

http://identifiers.org/hco/2/GRCh38#105420426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43219013-C-A

105420426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219013-C-T

105420492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219081-A-G

105420505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219097-A-G

http://identifiers.org/hco/2/GRCh38#105421097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43219132-C-A

105421099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219134-G-A

105421131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219162-C-T

105421161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219192-G-A

105421215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219245-A-G

105421289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219327-G-A

105421376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219413-G-A

105421775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219813-A-G

http://identifiers.org/hco/2/GRCh38#105421785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43219823-C-A

105421785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219823-C-T

105421794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219832-T-C

105421914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219952-T-C

105421937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43219983-T-C

105422057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220100-G-A

105422667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220643-G-A

105422667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220643-G-T

http://identifiers.org/hco/2/GRCh38#105422671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43220647-C-A

105422675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220651-T-G

105422829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220792-A-G

105422951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220914-A-G

105422991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220948-C-T

105422992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220949-G-A

105422992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43220949-G-T

105423356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43221310-G-C

105423530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43221646-C-G

http://identifiers.org/hco/2/GRCh38#105426154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43221779-C-A

105426195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43221820-A-T

http://identifiers.org/hco/2/GRCh38#105426300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43221924-C-A

http://identifiers.org/hco/2/GRCh38#105426433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43222056-A-C

105426433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222056-A-G

http://identifiers.org/hco/2/GRCh38#105426443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43222065-A-C

105426443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222065-A-G

105426504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222116-C-G

105426517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222129-C-T

105426524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222136-G-T

http://identifiers.org/hco/2/GRCh38#105426530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43222146-C-A

105426530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222146-C-T

105426625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222245-G-A

105426692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222310-G-C

105426720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222338-A-G

105426752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222368-A-G

105426904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222513-A-G

105426911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222520-T-C

105426911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43222520-T-G

105426982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223223-C-T

105427017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223249-C-G

105427120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223337-G-A

105427209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223425-T-G

105427215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223431-C-T

105427229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223442-T-A

http://identifiers.org/hco/2/GRCh38#105427365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43223572-C-A

105427402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223604-C-G

105427670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43223819-T-C

http://identifiers.org/hco/2/GRCh38#105427962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -C-A

105428032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -G-A

105428037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -G-A

105428251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -C-T

105428270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: -G-A

105428427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43226656-A-G

http://identifiers.org/hco/2/GRCh38#105428563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43226784-C-A

105428563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43226784-C-G

http://identifiers.org/hco/2/GRCh38#105428825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43227054-C-A

http://identifiers.org/hco/2/GRCh38#105428915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43227147-C-A

105429051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43227253-T-C

http://identifiers.org/hco/2/GRCh38#105429056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43227258-C-A

105429056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43227258-C-T

105429085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43227285-G-C

105429095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43227295-A-G

105429169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43227376-A-G

105429196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43227410-C-T

105431606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229067-G-A

105431611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229072-C-T

105431633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229096-T-G

105431717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229176-C-T

105431741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229200-G-A

105431996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229577-T-C

105432013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229594-T-C

105432020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229601-A-G

105432218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229779-A-T

105432356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43229883-C-G

105432785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230189-A-T

105432837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230253-A-G

105432877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230275-A-T

105432885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230283-A-G

105432909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230307-G-C

105432922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230320-C-T

105433772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230835-G-A

105433833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230891-G-A

105433834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230892-A-T

105433836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230894-T-A

105433901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43230959-T-C

105434022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43231077-C-G

105434022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43231077-C-T

http://identifiers.org/hco/2/GRCh38#105434056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43231112-C-A

105434066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43231122-T-C

105436127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43231727-C-T

105436145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43231745-A-G

105436226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43231971-T-A

105436260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43232066-G-T

105436261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43232067-T-G

105436291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43232097-C-G

http://identifiers.org/hco/2/GRCh38#105436310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43232116-A-C

105436367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43232166-T-C

105436480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43232279-G-A

105436480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43232279-G-T

http://identifiers.org/hco/2/GRCh38#105437155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43234464-C-A

http://identifiers.org/hco/2/GRCh38#105437240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43234884-A-C

105437336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43234940-C-G

105437336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43234940-C-T

105437894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43235376-C-T

http://identifiers.org/hco/2/GRCh38#105437962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43235443-C-A

105438006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43235492-A-G

105438142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43235595-C-T

105438250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43235636-G-T

105438322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43235698-T-A

105438322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43235698-T-C

105438385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: intron variant
orthologous variants: 43235777-C-T

105438412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5 prime UTR variant
orthologous variants: 43235824-G-T

105438414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5 prime UTR variant
orthologous variants: 43235833-T-C

105438441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5 prime UTR variant
orthologous variants: 43235860-G-A

105438441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5 prime UTR variant
orthologous variants: 43235860-G-T

http://identifiers.org/hco/2/GRCh38#105438490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3703
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#43235919-C-A