18545775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3 prime UTR variant
orthologous variants: 15000986-C-T

18545806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3 prime UTR variant
orthologous variants: 15001025-G-A

18545806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3 prime UTR variant
orthologous variants: 15001025-G-T

http://identifiers.org/hco/10/GRCh38#18545837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15001054-C-A

http://identifiers.org/hco/10/GRCh38#18545927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15001143-C-A

18545927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3 prime UTR variant
orthologous variants: 15001143-C-T

18546005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: synonymous variant
orthologous variants: 15001217-G-A

18546005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: missense variant
orthologous variants: 15001217-G-T

18546065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15001277-T-A

18546065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15001277-T-C

18546199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001411-G-A

18546199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001411-G-T

18546244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001453-A-G

18547099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001922-A-G

18547344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002125-T-C

18547425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002205-G-T

http://identifiers.org/hco/10/GRCh38#18547489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15002268-A-C

18547491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002270-G-A

18547603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002356-T-C

18547763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002513-A-T

18548025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002902-T-C

18548025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002902-T-G

18548180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15003046-G-C

18548250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003116-G-A

http://identifiers.org/hco/10/GRCh38#18548255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15003121-C-A

18548294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003160-G-A

18548294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003160-G-T

http://identifiers.org/hco/10/GRCh38#18548378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15003242-A-C

18548378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003242-A-G

http://identifiers.org/hco/10/GRCh38#18548413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15003269-C-A

18548705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003527-C-G

18549874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15012336-T-C

18549971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15012428-A-T

18550023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15012480-C-T

18550144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15012629-T-C

18550276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15012760-C-T

18550450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15012930-G-C

http://identifiers.org/hco/10/GRCh38#18550486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15012968-A-C

18551098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15013488-G-C

18551577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15013994-A-G

http://identifiers.org/hco/10/GRCh38#18551652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15014056-C-A

18551652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15014056-C-G

18551664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15014066-A-G

18551986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014385-A-G

http://identifiers.org/hco/10/GRCh38#18552083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15014505-A-C

http://identifiers.org/hco/10/GRCh38#18552105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15014527-C-A

18552105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014527-C-T

18552108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014530-G-A

18552108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014530-G-T

http://identifiers.org/hco/10/GRCh38#18552137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15014558-C-A

18552137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014558-C-T

http://identifiers.org/hco/10/GRCh38#18552187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15014604-A-C

18552373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014804-A-T

18552425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014860-T-C

http://identifiers.org/hco/10/GRCh38#18552426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15014861-A-C

18552426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15014861-A-G

http://identifiers.org/hco/10/GRCh38#18585447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15017453-C-A

18585447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15017453-C-T

18585772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15017742-C-T

18585830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15017800-A-G

18585912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15017908-T-C

18585916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15017912-T-C

18585970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: missense variant
orthologous variants: 15017972-C-G

18585970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: missense variant
orthologous variants: 15017972-C-T

18585980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: synonymous variant
orthologous variants: 15017982-C-T

18586135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15018110-A-G

18586169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15018149-G-A

18586169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15018149-G-C

18586169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15018149-G-T

18586180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15018160-G-A

http://identifiers.org/hco/10/GRCh38#18586193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15018173-C-A

18586193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15018173-C-T

http://identifiers.org/hco/10/GRCh38#18586201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15018179-C-A

18586201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15018179-C-T

http://identifiers.org/hco/10/GRCh38#18587126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15018379-C-A

18587201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15018449-G-A

18587388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15018621-A-T

18594825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15032037-C-T

18594856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15032065-C-T

http://identifiers.org/hco/10/GRCh38#18595109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15032266-C-A

http://identifiers.org/hco/10/GRCh38#18595131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15032288-C-A

http://identifiers.org/hco/10/GRCh38#18595850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15034524-A-C

18595859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034533-T-A

18595859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034533-T-C

18595875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034549-T-C

18595882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034556-T-A

18596022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034696-T-C

18596078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034744-A-G

18596092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034756-T-A

18596092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034756-T-C

http://identifiers.org/hco/10/GRCh38#18596108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15034769-C-A

18596110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034771-G-T

18596191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15034824-T-C

18607287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15036328-T-A

18607331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15036382-A-G

18608165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15039807-C-G

http://identifiers.org/hco/10/GRCh38#18608713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15040278-C-A

18608713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040278-C-T

18608736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040300-G-C

18609007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040525-T-C

18609021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040539-G-A

18609118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040588-G-A

18609721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040984-G-A

18609721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040984-G-C

18609733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15040996-T-C

18609750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15041010-G-C

18609750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15041010-G-T

18609821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15041074-T-C

18609954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15041195-C-T

18610610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, undefined
orthologous variants: 15041666-C-T

18610632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, undefined
orthologous variants: 15041688-G-A

18610687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15041727-G-C

18613528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15041912-C-T

18613530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15041914-T-C

18613670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042005-G-A

18613681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042017-T-C

18613758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042090-A-T

18613791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042119-C-T

18613998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042335-C-T

18614031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042368-T-C

18614286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042709-T-A

18614340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042774-T-A

18614340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042774-T-C

18614340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042774-T-G

18614374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042800-T-A

18614374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042800-T-C

18614423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042848-A-G

18614435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15042860-T-C

http://identifiers.org/hco/10/GRCh38#18614476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#15042901-C-A

18614519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: synonymous variant
orthologous variants: 15042944-A-G

http://identifiers.org/hco/10/GRCh38#18614569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#15042994-C-A

18614765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15043194-T-C

18615619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15043682-C-G

18615619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15043682-C-T

http://identifiers.org/hco/10/GRCh38#18615725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15043763-C-A

18615798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15043817-G-C

18615832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, undefined
orthologous variants: 15043844-G-C

http://identifiers.org/hco/10/GRCh38#18616092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15044482-A-C

18616121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15044493-T-A

18616133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15044505-T-A

18616133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15044505-T-C

18616133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15044505-T-G

18616300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 15044660-A-G

18640403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15045885-T-C

18640403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15045885-T-G

http://identifiers.org/hco/10/GRCh38#18642360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15046934-C-A

http://identifiers.org/hco/10/GRCh38#18642399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15046965-C-A

18642399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15046965-C-G

http://identifiers.org/hco/10/GRCh38#18642427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15046990-C-A

18642428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15046991-A-G

18642610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15047232-T-C

18642618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15047240-C-G

18642633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15047255-A-G

18643472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15048464-T-C

18643604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15048591-A-G

18643612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15048603-A-G

18643735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15048725-T-C

18643735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15048725-T-G

http://identifiers.org/hco/10/GRCh38#18643742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15048732-C-A

18646431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15050056-G-A

18646489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15050127-C-T

18646852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15050186-G-T

18646870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15050201-C-G

18647146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15050430-T-C

18647146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15050430-T-G

18650059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15052598-T-C

18650059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15052598-T-G

18650206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15052746-G-A

18650206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15052746-G-C

18650692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053321-C-G

18650986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053618-A-G

18650999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053631-T-C

http://identifiers.org/hco/10/GRCh38#18651003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15053638-C-A

18651003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053638-C-T

http://identifiers.org/hco/10/GRCh38#18651029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15053664-C-A

18651029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053664-C-T

18651044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053674-C-G

18651044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053674-C-T

18651088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053701-A-G

http://identifiers.org/hco/10/GRCh38#18651125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15053729-C-A

18651125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053729-C-G

18651125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron variant
orthologous variants: 15053729-C-T

18651204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15053808-T-A

18651204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15053808-T-C

18651211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15053815-G-C

18651211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15053815-G-T

http://identifiers.org/hco/10/GRCh38#18651570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#15054064-C-A

18651570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15054064-C-T

http://identifiers.org/hco/10/GRCh38#18651658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#15054149-C-A

18651658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15054149-C-G

18651658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15054149-C-T

http://identifiers.org/hco/10/GRCh38#18651676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#15054167-C-A

18651676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15054167-C-G

18651676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15054167-C-T

http://identifiers.org/hco/10/GRCh38#18651707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#15054194-C-A

18651707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15054194-C-G

18651707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15054194-C-T

18652074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054553-A-G

18652129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054598-C-G

18652129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054598-C-T

18652155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054624-G-A

http://identifiers.org/hco/10/GRCh38#18652174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15054628-C-A

18652174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054628-C-G

18652202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054652-A-T

18652343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054804-A-G

18652380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054841-A-G

18653795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15055932-A-G

18654475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15056746-A-T

18654527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15056796-G-A

18654537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15056804-T-A

18654921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15056881-G-T

http://identifiers.org/hco/10/GRCh38#18655036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15056990-C-A

18655058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15057012-G-C

http://identifiers.org/hco/10/GRCh38#18655145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15057090-C-A

18655145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 15057090-C-T

http://identifiers.org/hco/10/GRCh38#18655147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15057092-C-A

18655147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 15057092-C-G

18655219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057164-T-A

18655219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057164-T-C

18655308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057265-G-A

18655308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057265-G-T

18655483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057443-A-G

18655604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057555-C-T

18655658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057622-G-A

18655677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057642-A-T

18655747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057705-T-A

18655902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15057868-C-T

18656687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15058420-G-A

18657243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15058937-G-T

http://identifiers.org/hco/10/GRCh38#18657405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15059062-C-A

18657405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059062-C-T

18657689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059323-C-T

18657706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059340-C-T

18657758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059391-C-T

18657763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059396-G-A

http://identifiers.org/hco/10/GRCh38#18658187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15059135-C-A

http://identifiers.org/hco/10/GRCh38#18658279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15059231-C-A

18658343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059344-T-C

18658388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059412-G-A

18658388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059412-G-T

18658396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059420-A-T

18658419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059436-C-T

18658429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059453-A-T

18658442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059466-G-T

18658455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059479-G-A

18658467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059492-G-T

http://identifiers.org/hco/10/GRCh38#18658468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15059493-C-A

18658468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15059493-C-T

18658604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059626-G-A

18658604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059626-G-C

18658604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059626-G-T

18659075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059833-T-C

18659075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059833-T-G

18659143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059881-A-G

18659153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059891-G-A

18659153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059891-G-C

http://identifiers.org/hco/10/GRCh38#18659183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#15059925-C-A

18659183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059925-C-G

18659183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 15059925-C-T

18659187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059929-C-G

18659187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15059929-C-T

http://identifiers.org/hco/10/GRCh38#18659244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#15059980-C-A

18659244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15059980-C-T

http://identifiers.org/hco/10/GRCh38#18659263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#15059999-A-C

18659263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15059999-A-G

18659263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15059999-A-T

18659325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5 prime UTR variant
orthologous variants: 15060061-T-A

18659325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23529
most severe consequence: 5 prime UTR variant
orthologous variants: 15060061-T-C