http://identifiers.org/hco/1/GRCh38#246839280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179572421-C-A

246839280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179572421-C-G

246839280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179572421-C-T

246839540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179572691-A-G

246839623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179572780-G-T

http://identifiers.org/hco/1/GRCh38#246839720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179572867-C-A

246839720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179572867-C-T

246839808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179572955-T-C

http://identifiers.org/hco/1/GRCh38#246839890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179573026-A-C

246840048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573179-G-A

246840073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573189-A-T

246840128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573236-C-T

246840195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573302-A-G

246840234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573344-T-C

246840416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573522-T-C

246840439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573544-G-T

246840508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179573625-C-T

246841477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179574401-G-A

246841523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179574436-T-C

246841630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179574537-A-T

246843881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179576208-A-G

246843909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179576236-A-G

246843910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179576237-G-A

246843910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179576237-G-T

246843911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179576238-G-A

246843911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179576238-G-T

246844058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179576391-T-C

246844078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179576418-T-C

246844078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179576418-T-G

246844211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179576553-T-G

http://identifiers.org/hco/1/GRCh38#246844285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179576607-C-A

246849637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179579904-T-C

246849790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580057-C-G

246849796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580063-A-T

246849800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580067-G-A

246849800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580067-G-C

246849803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580070-C-T

246849804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580071-G-A

246849804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580071-G-T

246849820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179580084-G-A

246849820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580084-G-C

246849820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580084-G-T

246849826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179580090-T-A

246849826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179580090-T-C

246849835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179580099-T-C

246849865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580129-T-A

246849865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179580129-T-C

246849865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580129-T-G

246849866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580130-T-C

246850274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580511-A-G

246850276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179580513-A-G

246850392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580629-G-A

246850536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179580773-C-T

246850585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179580819-A-G

246850821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581028-T-C

246850821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581028-T-G

246850830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581037-T-C

246850841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581048-C-G

246850845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581052-T-C

246850896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581103-T-C

246851006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581213-G-A

246851006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581213-G-C

246851006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581213-G-T

246851032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179581239-T-C

246851121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581328-T-C

246851131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581338-T-G

246851145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581352-C-T

246851169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581364-C-T

246851226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581421-A-T

246851273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179581468-A-G

http://identifiers.org/hco/1/GRCh38#246851473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179581670-A-C

http://identifiers.org/hco/1/GRCh38#246851487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179581684-A-C

246851547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179581750-T-A

246851547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179581750-T-C

246851840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179581992-T-A

246851840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179581992-T-C

246851840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179581992-T-G

http://identifiers.org/hco/1/GRCh38#246851851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179582003-C-A

246851871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179582022-C-T

246852647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179582718-T-G

246853025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179582954-G-A

246853025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179582954-G-C

246853025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179582954-G-T

http://identifiers.org/hco/1/GRCh38#246853120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179583043-C-A

246853120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179583043-C-T

246853155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179583078-C-T

http://identifiers.org/hco/1/GRCh38#246853342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179583284-A-C

246853342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179583284-A-T

http://identifiers.org/hco/1/GRCh38#246853381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179583313-C-A

246853381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179583313-C-T

http://identifiers.org/hco/1/GRCh38#246853386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179583318-C-A

246855636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179585450-A-G

http://identifiers.org/hco/1/GRCh38#246855750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179585520-A-C

246855809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179585576-C-G

http://identifiers.org/hco/1/GRCh38#246855930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179585680-A-C

246855930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179585680-A-G

246856083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179585851-G-A

246856083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179585851-G-T

246856302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179586037-A-G

246856330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179586057-T-C

http://identifiers.org/hco/1/GRCh38#246856471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179586220-A-C

246857712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179587848-C-T

246857839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179587951-T-C

http://identifiers.org/hco/1/GRCh38#246857925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179587997-A-C

246857925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179587997-A-T

246857926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179587998-G-A

246857926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179587998-G-T

http://identifiers.org/hco/1/GRCh38#246857935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179588007-C-A

246857935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179588007-C-T

246858337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179588093-G-C

246858426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179588174-A-T

246859175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179588576-C-T

246859973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179589758-A-G

http://identifiers.org/hco/1/GRCh38#246860813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179590026-C-A

246860813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179590026-C-T

246860827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179590040-G-C

246860827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179590040-G-T

246860926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179590137-T-A

246860927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179590138-T-A

246860927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179590138-T-G

246860944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179590155-C-T

246861325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179590543-A-T

http://identifiers.org/hco/1/GRCh38#246861387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179590601-C-A

246861387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179590601-C-T

246861974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179591050-T-A

246861978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179591054-T-G

http://identifiers.org/hco/1/GRCh38#246862007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179591083-A-C

246862075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179591160-G-C

246862214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179591334-C-T

246862237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179591356-T-C

246862237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179591356-T-G

246862250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179591369-G-A

246862250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179591369-G-T

246862267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179591393-T-G

246862294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179591435-C-T

246863197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179592153-G-A

246863197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179592153-G-T

246863441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

246863710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

246864089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179593608-G-A

246864089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179593608-G-T

246864237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179593711-T-C

http://identifiers.org/hco/1/GRCh38#246864251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179593724-C-A

246866069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

246866336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

246867073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179595724-C-G

http://identifiers.org/hco/1/GRCh38#246867104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179595756-C-A

246867164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179595809-A-T

246867175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179595820-T-A

246867175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179595820-T-C

246867364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179595980-A-G

246867450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596076-T-C

246867473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596101-T-C

http://identifiers.org/hco/1/GRCh38#246867483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179596111-C-A

246867495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596221-A-G

246867495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596221-A-T

246867498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596224-G-A

246867498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596224-G-T

246867548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596297-T-A

246867568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596317-C-G

246867795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179596688-T-C

246867795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179596688-T-G

http://identifiers.org/hco/1/GRCh38#246867859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179596748-A-C

http://identifiers.org/hco/1/GRCh38#246876001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179596842-C-A

246876001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179596842-C-G

http://identifiers.org/hco/1/GRCh38#246876221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179597052-C-A

246876221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179597052-C-T

246876270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179597098-C-T

246876277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179597105-T-A

http://identifiers.org/hco/1/GRCh38#246876321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179597143-C-A

246876321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179597143-C-G

246876321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179597143-C-T

246876598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179597886-A-G

246876608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179597896-T-C

246876849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179598053-G-C

246876849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179598053-G-T

http://identifiers.org/hco/1/GRCh38#246876850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179598054-C-A

246876850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179598054-C-T

246876909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179598113-T-C

246877242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179598448-C-G

246877242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179598448-C-T

246877770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179599109-T-C

246877840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179599172-T-A

246877854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179599185-T-C

246884725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179602539-A-G

246885425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179602834-C-G

246885606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179603010-T-C

246885713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179603114-T-C

246885770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179603183-C-T

246885774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179603187-A-G

246887217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179603579-G-A

246887410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179603765-G-A

246887410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179603765-G-T

http://identifiers.org/hco/1/GRCh38#246887450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179603800-A-C

246887450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179603800-A-G

http://identifiers.org/hco/1/GRCh38#246888075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179604975-C-A

246888097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605003-G-A

246888097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605003-G-C

246888097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605003-G-T

246888109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605015-T-C

246888165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605056-T-G

246888377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605249-C-G

246888577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605450-C-T

246888583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605456-T-A

246888583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605456-T-C

246888925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605499-T-C

246889010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605578-A-G

246889018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605585-A-G

246889054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605616-C-T

246889333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605831-G-C

246889486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179605973-T-C

246889828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179606401-T-A

246890046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179607249-C-G

246890046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179607249-C-T

246890188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179607497-G-A

246890188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179607497-G-T

http://identifiers.org/hco/1/GRCh38#246890211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179607523-C-A

246890716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608254-T-A

246890716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608254-T-C

246890789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608311-T-C

246890859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608341-T-A

246890859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608341-T-G

246890950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608415-T-C

http://identifiers.org/hco/1/GRCh38#246890975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179608440-C-A

246890975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179608440-C-T

246891089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608562-T-C

246891103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608585-T-C

http://identifiers.org/hco/1/GRCh38#246891114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179608596-C-A

246891502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608869-C-G

246891502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179608869-C-T

246891682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609127-A-G

246891687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609132-G-A

246891687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609132-G-T

246891689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609134-T-A

http://identifiers.org/hco/1/GRCh38#246891751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179609184-C-A

246891751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609184-C-T

http://identifiers.org/hco/1/GRCh38#246891897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179609326-C-A

246891897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179609326-C-T

http://identifiers.org/hco/1/GRCh38#246891960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179609388-A-C

246891960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609388-A-T

246892040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609444-T-A

246892058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179609462-A-T

246894828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179610690-G-A

246894828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179610690-G-T

246894981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179610828-G-A

246895273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179611234-T-C

http://identifiers.org/hco/1/GRCh38#246895824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179611644-C-A

246898463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179612778-T-C

http://identifiers.org/hco/1/GRCh38#246898477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179612794-A-C

246898863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179613085-G-A

246898885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179613098-C-G

246898885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179613098-C-T

http://identifiers.org/hco/1/GRCh38#246898890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179613103-C-A

246898890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179613103-C-T

246899526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179613714-T-A

246899526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179613714-T-G

246900003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179614212-T-A

246900003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179614212-T-C

246900210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179614405-T-C

http://identifiers.org/hco/1/GRCh38#246900250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179614445-A-C

246900250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 179614445-A-G

246900312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179614508-G-A

246901051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615186-A-G

246902142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615414-C-T

246902236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615497-T-C

246902413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615654-A-T

http://identifiers.org/hco/1/GRCh38#246902467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179615699-C-A

246902467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615699-C-G

246902467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615699-C-T

246902503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615730-T-C

246902743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615966-T-A

246902743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179615966-T-C

246902796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179616002-G-T

http://identifiers.org/hco/1/GRCh38#246903906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179617172-C-A

246903972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179617237-C-G

246904073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179617335-T-A

246904073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179617335-T-C

246904124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179617378-G-A

246904124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179617378-G-T

246904485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179617618-C-T

246905897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179618220-G-A

246906156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179618725-A-G

246906243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179618819-A-G

246907363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179619768-T-C

246907519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179619880-A-G

246907523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179619884-T-A

246907523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179619884-T-C

246907523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179619884-T-G

246913260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179621236-T-A

246913260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179621236-T-C

246913326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179621302-T-A

246913326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179621302-T-C

246913524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179621487-G-A

246913524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179621487-G-C

246913524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179621487-G-T

246913554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179621524-G-A

246913554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179621524-G-T

246913878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179622008-T-C

http://identifiers.org/hco/1/GRCh38#246913918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179622046-A-C

246916076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179623183-A-G

246916339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179623439-T-C

246918329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179626855-T-C

246918407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179626933-T-C

246918407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179626933-T-G

246928779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179628666-T-C

246928937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179628826-T-C

246928937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179628826-T-G

246929167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629017-G-A

246929478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629131-T-A

246929478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629131-T-G

246929489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629142-G-A

246929550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629190-T-C

246929635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629271-T-C

246929776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629351-G-A

246929792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629367-G-A

246929811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629386-T-C

246929836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629421-G-A

246929864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629452-C-T

246929886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629474-T-C

246930808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179629986-G-A

http://identifiers.org/hco/1/GRCh38#246930963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179630394-C-A

http://identifiers.org/hco/1/GRCh38#246930983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#179630414-C-A

246930983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179630414-C-T

http://identifiers.org/hco/1/GRCh38#246931542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#179630890-C-A

http://identifiers.org/hco/1/GRCh38#246931562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179630902-C-A

246931562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179630902-C-G

246931562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179630902-C-T

http://identifiers.org/hco/1/GRCh38#246931714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#179631015-C-A

246931714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 179631015-C-T

246931847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 179631107-G-A

246931847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 179631107-G-T

246931888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24618
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 179631141-T-G