15617481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: 141450701-G-A

15617481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: 141450701-G-C

15617481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: 141450701-G-T

http://identifiers.org/hco/1/GRCh38#15617497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141450685-A-C

15617497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: 141450685-A-G

15617497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: 141450685-A-T

http://identifiers.org/hco/1/GRCh38#15617520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141450662-C-A

15617520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: 141450662-C-T

15617540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5 prime UTR variant
orthologous variants: 141450642-G-T

http://identifiers.org/hco/1/GRCh38#15617601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141450568-C-A

15617601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141450568-C-T

15617607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141450562-C-G

15617607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141450562-C-T

15617631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141450538-G-T

15617641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141450528-A-G

15617647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141450522-G-A

15617647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 141450522-G-T

15617795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141450379-C-T

15618137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141450197-G-A

15618137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141450197-G-C

15618247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141450119-T-C

http://identifiers.org/hco/1/GRCh38#15618357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141450019-C-A

15618504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141449870-T-A

15618641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141449752-G-C

15618778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141449621-C-T

15619458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141449005-T-C

15619487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448964-A-T

15619600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448888-T-C

15619643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448837-A-G

15619796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448769-C-G

15620032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448512-T-C

15620142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448418-A-T

15620144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448416-T-C

http://identifiers.org/hco/1/GRCh38#15620473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141448084-C-A

15620522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141448053-C-T

15620699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141447887-T-G

15620754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141447827-T-C

15622627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141445612-A-G

15622627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141445612-A-T

15624218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141443369-T-C

15624499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141443158-C-T

15624506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141443151-G-A

15624550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141443110-C-T

http://identifiers.org/hco/1/GRCh38#15624591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141443078-C-A

15624990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141442880-A-G

15625024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141442847-A-G

15625165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

15625224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141442604-C-T

15625346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141442490-T-G

15625502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141442350-T-A

15626202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141441835-C-T

15626502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440980-C-T

15626540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440942-A-T

15626617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440883-G-A

15626617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440883-G-T

15626635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440865-G-A

15626650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440854-A-G

http://identifiers.org/hco/1/GRCh38#15626684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141440820-A-C

15626684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141440820-A-G

15626741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141440763-G-A

15626744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141440760-G-T

15626854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141440653-C-T

15626939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141440590-T-C

http://identifiers.org/hco/1/GRCh38#15626974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141440540-C-A

http://identifiers.org/hco/1/GRCh38#15627160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141440388-C-A

15627160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440388-C-T

15627258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141440308-G-A

15627505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438805-T-C

15627566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438748-A-G

15627792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438535-G-C

15627855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438485-T-C

15627934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438422-A-G

15627981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438405-T-C

15628159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438204-A-T

15628228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141438141-A-T

15630229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141435859-G-A

15630229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141435859-G-C

15630229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141435859-G-T

15630239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141435849-A-G

15630247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141435843-G-A

15630247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141435843-G-T

15630570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141435520-A-G

http://identifiers.org/hco/1/GRCh38#15630584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141435506-C-A

15630584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141435506-C-G

15630584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141435506-C-T

15630590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141435500-G-T

15630594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141435496-G-C

15630594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141435496-G-T

15632801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141434107-G-C

15633476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141433330-C-G

15633742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141433103-T-C

15633830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141433032-A-G

http://identifiers.org/hco/1/GRCh38#15633894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141432986-C-A

15633894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141432986-C-T

15634212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141432708-G-A

http://identifiers.org/hco/1/GRCh38#15634227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141432693-C-A

15634283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141432638-T-A

15634389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141432558-A-G

15634390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141432557-C-T

15634524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141432446-T-A

15634626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141432342-C-G

15634626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141432342-C-T

15638123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141430722-G-A

15638192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141430644-G-T

15638199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141430637-T-C

15638208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141430628-A-G

15638226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141430610-T-C

15638237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141430599-T-C

15638284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141430569-T-C

15640240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141428583-T-C

15640330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141428523-T-G

15640505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141428389-A-G

15640520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141428378-G-A

15640536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141428364-C-T

15640803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141428154-A-G

15640823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141428126-G-A

15641235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141427723-G-A

15641235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141427723-G-T

15641491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141427500-A-G

15641590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141427408-T-A

15643510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141426179-C-T

15643669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141426022-G-A

15651902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141419557-G-A

15652011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141419479-G-T

15652017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141419473-G-A

15652017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141419473-G-T

15652030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141419464-G-C

15652030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141419464-G-T

http://identifiers.org/hco/1/GRCh38#15652047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141419448-C-A

15652047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141419448-C-G

15652047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141419448-C-T

15654760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141417948-G-A

http://identifiers.org/hco/1/GRCh38#15654885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141417874-A-C

15655119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141417711-G-A

15655152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141417683-T-C

15655265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141417574-G-C

15655489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141417364-C-T

15655509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141417345-T-C

http://identifiers.org/hco/1/GRCh38#15656712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141416549-C-A

15656818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141416448-G-A

15656818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141416448-G-T

http://identifiers.org/hco/1/GRCh38#15656837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141416429-C-A

15656837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141416429-C-T

http://identifiers.org/hco/1/GRCh38#15656912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141416351-C-A

15656927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141416296-T-C

http://identifiers.org/hco/1/GRCh38#15656989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141416225-C-A

15657022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141416195-G-T

http://identifiers.org/hco/1/GRCh38#15657074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141416156-C-A

15657074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141416156-C-T

15657099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141416140-G-T

15657131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141416111-A-G

15657352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141415733-A-G

15657524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141415592-C-T

15657642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141415494-A-G

15659219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141413656-T-C

15659231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141413643-C-G

15659398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 141413496-G-T

15659820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 141412953-C-T

http://identifiers.org/hco/1/GRCh38#15659944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141412836-C-A

15659944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412836-C-T

15660072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412708-G-T

15660157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412638-A-G

15660157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412638-A-T

15660160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412635-C-G

15660188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412607-C-G

15660188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412607-C-T

15660215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412580-G-A

15660288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412507-G-A

15660288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412507-G-C

15660306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412489-T-G

15660348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412447-T-A

15660393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412402-G-C

15660394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412401-T-C

15660394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412401-T-G

15660705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141412114-T-G

15660869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141411953-T-A

15660869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141411953-T-G

15660878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141411944-G-A

15660878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141411944-G-C

http://identifiers.org/hco/1/GRCh38#15660998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141411824-A-C

15661052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 141411770-T-C

15661063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 141411759-T-C

http://identifiers.org/hco/1/GRCh38#15661233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141411592-C-A

15661233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 141411592-C-G

15661233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 141411592-C-T

15661473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 141411406-G-T

15661588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 141411294-G-T

15661747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141411136-T-C

15661789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141411100-C-G

15661789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141411100-C-T

15661816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141411079-C-T

15661877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141411027-G-A

15661877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141411027-G-T

15661887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141411017-A-G

15661925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410982-T-C

15661930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410977-A-T

15661939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410968-G-T

15661992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410917-A-G

15662024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410882-G-A

15662044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410862-G-T

15662078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410831-T-A

15662078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410831-T-C

http://identifiers.org/hco/1/GRCh38#15662094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141410816-C-A

http://identifiers.org/hco/1/GRCh38#15662095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141410815-C-A

15662123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410790-A-G

15662125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410788-A-T

15662130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410783-G-A

15662130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410783-G-T

15662135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410780-T-C

15662154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410761-A-G

15662155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410760-G-A

15662155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410760-G-T

15662300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410673-G-A

15662300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410673-G-C

15662314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410659-G-T

15662342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410632-G-T

15662352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410622-A-G

15662354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410620-G-A

http://identifiers.org/hco/1/GRCh38#15662369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141410605-C-A

15662370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410604-T-C

15662376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410594-G-A

15662376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410594-G-T

15662386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410584-G-T

15662387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410583-G-T

15662398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410568-G-T

15662401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410565-T-C

15662439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410530-G-T

15662447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410522-C-T

15662451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410518-G-T

http://identifiers.org/hco/1/GRCh38#15662452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141410517-C-A

15662460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410509-A-G

15662461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410508-C-G

15662483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410486-A-G

15662517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410444-G-A

15662538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410425-A-G

15662542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410421-T-C

15662542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410421-T-G

15662580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410381-T-C

15662581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410380-A-G

15662608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410356-T-C

15662646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410339-C-G

15662646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410339-C-T

15662647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410338-A-G

15662648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410337-T-C

15662742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410231-T-A

15662801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141410183-T-C

15663240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409743-T-C

15663386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409620-C-T

15663425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409581-G-T

15663463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409544-T-A

15663475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409532-G-T

15663568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409439-T-C

15663579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409428-G-C

http://identifiers.org/hco/1/GRCh38#15663723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141409311-C-A

15663723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409311-C-T

http://identifiers.org/hco/1/GRCh38#15663844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141409203-C-A

15663844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409203-C-T

15663858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409192-G-T

15663991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141409029-A-G

15664249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408901-G-A

15664294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408868-G-C

15664304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408860-G-A

http://identifiers.org/hco/1/GRCh38#15664432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141408783-C-A

15664507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408687-A-G

15664599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408631-T-C

15664676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408558-G-C

15664701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408534-G-A

http://identifiers.org/hco/1/GRCh38#15664733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141408502-C-A

15664733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408502-C-T

15664905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408410-A-G

http://identifiers.org/hco/1/GRCh38#15664911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141408404-C-A

15664911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408404-C-T

http://identifiers.org/hco/1/GRCh38#15664935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141408380-C-A

15664956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408359-T-A

15665314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408312-G-A

15665540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141408109-C-T

15665679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407985-G-A

15666057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407687-G-A

15666308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407436-G-T

15666310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407434-A-G

15666361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407393-G-A

15666361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407393-G-T

15666368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407386-A-G

15666573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407204-A-G

15666620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141407162-T-C

http://identifiers.org/hco/1/GRCh38#15666805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141406988-C-A

http://identifiers.org/hco/1/GRCh38#15666856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141406825-C-A

15666885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141406792-G-A

15666885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141406792-G-T

http://identifiers.org/hco/1/GRCh38#15666918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141406753-C-A

15667080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141406543-G-A

15667080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141406543-G-T

http://identifiers.org/hco/1/GRCh38#15667106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141406518-C-A

15667472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141406186-G-A

15667472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141406186-G-T

15667740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405999-G-A

15667740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405999-G-T

15667762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405987-A-G

15668032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405796-A-G

15668091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405737-G-T

15668098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405730-G-A

http://identifiers.org/hco/1/GRCh38#15668101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141405726-C-A

15668110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405717-G-T

15668719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405176-A-T

15668815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405086-A-G

15668815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24578
most severe consequence: 3 prime UTR variant
orthologous variants: 141405086-A-T