11479202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372339-G-A

11479202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372339-G-T

11479204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372337-T-C

11479204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372337-T-G

11479318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372220-C-T

11479343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372206-G-A

11479343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372206-G-T

11479363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372186-G-A

11479363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 148372186-G-T

11479378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148372172-T-A

11479378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148372172-T-C

11479390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148372159-G-T

11479462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148372100-C-T

11479511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148372042-G-A

11479511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148372042-G-T

11479782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148371785-A-G

11479835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148371731-T-C

http://identifiers.org/hco/1/GRCh38#11480095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148371464-A-C

11480323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148371283-A-G

11480602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148371035-T-C

11480711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148370959-A-G

11481007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148370703-C-G

11481111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148370647-C-T

11481132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148370626-C-T

http://identifiers.org/hco/1/GRCh38#11481227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148370543-C-A

11481227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148370543-C-T

11481271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370499-G-A

11481271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370499-G-C

11481271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370499-G-T

11481313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370456-T-A

11481313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370456-T-C

11481313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370456-T-G

11481401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370375-G-T

11481418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370311-A-G

11481563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370174-G-C

11481563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370174-G-T

11481641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148370097-C-T

11482077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148369776-G-A

11482289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148369638-T-C

11482306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148369621-A-G

http://identifiers.org/hco/1/GRCh38#11482413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148369536-A-C

11482432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148369520-C-T

11482547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148369430-G-A

11482717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148369258-C-G

11482864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148369127-C-T

11483140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148368849-C-T

11483154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148368836-G-A

11483285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148368707-C-G

11483447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148368545-G-A

11484124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, undefined
orthologous variants: 148367549-C-G

11484191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, undefined
orthologous variants: 148367450-A-G

11484198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148367443-C-T

11484402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, undefined
orthologous variants: 148367236-G-A

11484578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148367064-A-T

11484671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148366969-C-G

11484740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148366910-G-A

http://identifiers.org/hco/1/GRCh38#11484810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148366851-A-C

11485151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148366598-A-T

11485682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148366117-A-G

11485933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148365652-T-C

11486067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148365574-C-T

11486290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148365364-C-T

http://identifiers.org/hco/1/GRCh38#11486291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148365363-A-C

11486553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148365132-G-C

11486553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148365132-G-T

11487198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148364173-C-T

11487544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363922-C-T

11487721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363769-G-A

11487747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363744-C-G

11488028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363536-T-G

11488209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363371-A-T

http://identifiers.org/hco/1/GRCh38#11488234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148363346-C-A

11488277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363294-G-A

11488277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363294-G-C

11488484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363128-G-A

11488519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148363093-C-T

11488623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148362978-T-C

11488671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148362947-G-T

11489045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148362604-C-T

11489541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148362235-G-T

http://identifiers.org/hco/1/GRCh38#11489586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148362177-C-A

11489729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148362061-C-T

11489755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148362032-A-G

11489800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148361990-T-C

11490077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148361736-T-C

11490077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148361736-T-G

11490112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148361717-T-C

11492235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148360921-T-G

11492237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148360919-G-A

11492359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148360812-A-G

11492359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148360812-A-T

11492756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148360475-G-A

11492849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148360404-T-C

http://identifiers.org/hco/1/GRCh38#11494420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148359904-A-C

http://identifiers.org/hco/1/GRCh38#11494458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148359865-A-C

11494458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148359865-A-G

11499647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148358287-T-C

11500191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148357837-G-A

11500645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148357408-A-G

11500971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148356877-C-G

http://identifiers.org/hco/1/GRCh38#11501044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148356805-C-A

11501044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 148356805-C-T

11501046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148356803-G-A

http://identifiers.org/hco/1/GRCh38#11501084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148356777-C-A

11501152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 148356715-C-T

11501290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356577-G-A

11501290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356577-G-C

11501497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 148356370-T-G

11501523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 148356345-G-A

11501523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 148356345-G-T

http://identifiers.org/hco/1/GRCh38#11501615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148356282-C-A

11501620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148356277-C-T

http://identifiers.org/hco/1/GRCh38#11501728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148356256-C-A

11501728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356256-C-G

11501728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 148356256-C-T

http://identifiers.org/hco/1/GRCh38#11501750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148356234-C-A

11501750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356234-C-G

11501750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356234-C-T

11501767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356217-T-C

http://identifiers.org/hco/1/GRCh38#11501770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148356214-C-A

11501770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356214-C-G

11501779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356205-G-A

11501833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356151-G-C

11501833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356151-G-T

11501866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148356118-A-G

11501986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148355998-T-A

11502166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148355810-G-A

11502166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148355810-G-C

11502166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148355810-G-T

11502193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148355760-G-A

11502193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148355760-G-T

11502239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148355678-G-A

11502239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148355678-G-T

http://identifiers.org/hco/1/GRCh38#11502274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148355624-C-A

11502364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148355477-G-A

11502539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148355243-G-A

11502539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148355243-G-T

11502637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148355089-G-T

http://identifiers.org/hco/1/GRCh38#11502770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148354959-A-C

11502857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148354872-G-A

http://identifiers.org/hco/1/GRCh38#11502946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148354786-C-A

http://identifiers.org/hco/1/GRCh38#11502969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148354770-C-A

11502969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148354770-C-G

11502972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148354767-T-C

11502987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148354752-A-T

11503018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148354721-A-G

11514137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345892-A-G

11514272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345751-A-G

11514409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148345636-G-C

11514409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148345636-G-T

http://identifiers.org/hco/1/GRCh38#11514442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148345603-A-C

11514551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345487-C-G

11514551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345487-C-T

11514556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345482-T-A

11514563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345475-C-T

11514587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345463-G-T

http://identifiers.org/hco/1/GRCh38#11514588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148345462-C-A

11514588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345462-C-G

11514604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345446-T-C

11514803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345377-G-T

11514820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345360-G-A

11514885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345294-C-T

11515225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345204-T-A

11515225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345204-T-C

11515226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345203-G-A

11515226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345203-G-T

11515291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345152-T-A

11515291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345152-T-C

11515312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345131-G-T

11515318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345120-T-A

11515318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345120-T-C

11515318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345120-T-G

http://identifiers.org/hco/1/GRCh38#11515323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148345115-C-A

11515323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345115-C-T

11515352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148345086-T-C

11515404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148345034-C-G

11515572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344826-T-C

11515611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344798-G-A

11515611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344798-G-T

http://identifiers.org/hco/1/GRCh38#11515639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148344770-C-A

11515639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344770-C-T

11515756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344643-G-A

11515756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344643-G-C

11515761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344638-G-A

11515776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344623-G-A

11515776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344623-G-T

11515792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344610-G-T

11515793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344609-G-T

http://identifiers.org/hco/1/GRCh38#11515849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148344557-C-A

11515849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344557-C-T

11516009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148344437-G-A

11516033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148344413-T-G

http://identifiers.org/hco/1/GRCh38#11516199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148344246-C-A

11516223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344222-G-A

11516342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148344154-G-A

http://identifiers.org/hco/1/GRCh38#11516572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148343962-C-A

http://identifiers.org/hco/1/GRCh38#11516889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148343761-C-A

11517094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343586-C-T

11517156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343544-G-A

http://identifiers.org/hco/1/GRCh38#11517343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148343395-C-A

11517343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343395-C-G

11517348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343390-G-C

11517348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343390-G-T

11517390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343349-T-C

11517398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343341-G-A

11517398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343341-G-C

11517398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343341-G-T

11517450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343305-T-C

11517654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343105-A-G

11517728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343045-G-A

11517728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343045-G-T

11517748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343034-T-A

http://identifiers.org/hco/1/GRCh38#11517752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148343030-A-C

11517752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148343030-A-G

11517810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342986-A-G

11519162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342867-C-G

11519205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342834-A-G

11519243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342794-G-T

11519270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342769-T-A

11519292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342752-G-A

11519292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342752-G-T

http://identifiers.org/hco/1/GRCh38#11519300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148342744-C-A

11519300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342744-C-T

http://identifiers.org/hco/1/GRCh38#11519313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148342731-C-A

11519317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342728-A-G

11519432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148342615-G-A

11519569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342502-G-T

11519588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342483-T-A

11519601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342474-G-A

11519605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342470-G-A

11519623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342452-G-A

11519623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342452-G-T

11519642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342433-G-T

11519666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342418-A-G

11519667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342417-C-T

http://identifiers.org/hco/1/GRCh38#11519695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148342389-C-A

11519695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342389-C-T

11519718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: splice acceptor variant
orthologous variants: 148342366-G-A

11519767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148342317-G-A

11519767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148342317-G-T

http://identifiers.org/hco/1/GRCh38#11519930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148342146-A-C

http://identifiers.org/hco/1/GRCh38#11520003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148342093-C-A

11520003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342093-C-T

11520074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148342036-G-A

11520164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341948-G-A

11520277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341769-G-A

11520354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341720-C-T

11520514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341564-A-G

11520535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341542-T-C

http://identifiers.org/hco/1/GRCh38#11520537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148341540-C-A

11520537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341540-C-T

http://identifiers.org/hco/1/GRCh38#11520562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148341533-C-A

11520562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341533-C-G

11520562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341533-C-T

http://identifiers.org/hco/1/GRCh38#11520583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148341517-C-A

11520583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341517-C-T

11520584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341516-G-A

11520584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341516-G-T

http://identifiers.org/hco/1/GRCh38#11520596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148341504-C-A

11520658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341449-C-T

http://identifiers.org/hco/1/GRCh38#11520770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148341321-C-A

11520818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148341273-G-A

11520818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148341273-G-T

11520875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148341217-G-A

11521243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340992-G-T

11521277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340958-A-G

11521320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340925-G-A

http://identifiers.org/hco/1/GRCh38#11521332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148340913-A-C

11521382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340868-G-A

11521382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340868-G-T

11521498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340737-T-A

11521498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340737-T-C

11521498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148340737-T-G

11522355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148340395-G-T

11522389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148340365-C-T

http://identifiers.org/hco/1/GRCh38#11523805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148339808-C-A

11523805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339808-C-T

11523811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339802-A-G

http://identifiers.org/hco/1/GRCh38#11523855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148339773-C-A

11523861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339767-C-G

11523861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339767-C-T

11523916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339720-G-A

11524028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 148339603-G-A

11524028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 148339603-G-T

http://identifiers.org/hco/1/GRCh38#11524029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148339602-C-A

http://identifiers.org/hco/1/GRCh38#11524033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148339598-C-A

11524035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148339596-G-A

11524035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148339596-G-T

11524078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339560-G-A

http://identifiers.org/hco/1/GRCh38#11524087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148339551-C-A

11524087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339551-C-G

11524087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339551-C-T

11524122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339516-A-G

11524129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339509-A-G

11524158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339480-G-A

11524158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339480-G-T

11524188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339451-G-T

11524451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339210-A-G

11524564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339177-T-C

11524799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339110-C-T

11524837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339095-T-A

11524947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339050-T-A

11524947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148339050-T-C

11525050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338949-T-G

http://identifiers.org/hco/1/GRCh38#11525062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148338937-C-A

11525062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338937-C-G

11525062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338937-C-T

11525071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338928-G-A

http://identifiers.org/hco/1/GRCh38#11525079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148338920-C-A

11525079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338920-C-T

11525083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338916-T-C

11525086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338913-G-A

11525086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338913-G-T

11525372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338642-G-A

11525372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338642-G-T

11525447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338574-C-G

11525464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338557-A-G

http://identifiers.org/hco/1/GRCh38#11525518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148338515-C-A

11525577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338454-A-G

11525773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338275-T-A

11525822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338223-G-C

11525822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148338223-G-T

http://identifiers.org/hco/1/GRCh38#11526533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148337452-C-A

11526543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337442-G-A

11526543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337442-G-T

11526550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337435-G-A

11526847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337139-T-G

11526861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337128-G-T

11526881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337109-T-C

11526882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337108-T-G

11527639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148337076-T-C

11527842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148336899-C-G

http://identifiers.org/hco/1/GRCh38#11527876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148336860-C-A

11527876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148336860-C-T

11527896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148336827-A-T

11528145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336598-T-C

11528193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336562-A-G

http://identifiers.org/hco/1/GRCh38#11528293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148336471-C-A

11528363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336401-G-A

11528601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336211-G-T

http://identifiers.org/hco/1/GRCh38#11528767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148336148-C-A

11528767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336148-C-G

11528793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336137-C-G

11528828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336113-G-A

11528834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336107-C-G

11528905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148336041-C-T

11529228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148335791-C-G

11529264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148335762-C-T

11529367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148335662-C-T

http://identifiers.org/hco/1/GRCh38#11529434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148335593-C-A

http://identifiers.org/hco/1/GRCh38#11529435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148335592-A-C

11529435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148335592-A-G

http://identifiers.org/hco/1/GRCh38#11529481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148335566-C-A

11529481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148335566-C-T

11529526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148335521-G-A

11529526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148335521-G-T

11529611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148335415-G-A

11529730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335306-T-G

11529980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335056-A-G

11529985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335051-C-G

11529985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335051-C-T

11529991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335045-G-A

11529991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335045-G-T

http://identifiers.org/hco/1/GRCh38#11530055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148335029-C-A

11530055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335029-C-T

http://identifiers.org/hco/1/GRCh38#11530056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148335028-C-A

11530056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335028-C-G

11530056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335028-C-T

http://identifiers.org/hco/1/GRCh38#11530065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148335019-C-A

11530075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335009-G-A

11530075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148335009-G-T

http://identifiers.org/hco/1/GRCh38#11530076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148335008-C-A

http://identifiers.org/hco/1/GRCh38#11530101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148334983-A-C

11530101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334983-A-G

11530332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334828-T-C

11530733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334485-G-A

11530733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334485-G-T

http://identifiers.org/hco/1/GRCh38#11530768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148334459-C-A

11530768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334459-C-T

http://identifiers.org/hco/1/GRCh38#11530786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148334443-A-C

11530786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334443-A-G

11530850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334376-G-A

11530850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334376-G-C

11530877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334350-C-T

11530883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334344-C-G

11530979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148334250-A-G

11530982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148334247-G-A

11530982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148334247-G-T

11530990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148334239-C-G

11530990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 148334239-C-T

11530997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 148334232-C-T

11531059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334183-C-T

11531101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334159-T-C

11531124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334136-G-A

11531246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334035-C-T

11531256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148334025-G-A

11531445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148333857-G-T

11531480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148333820-T-G

11531506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, undefined
orthologous variants: 148333794-G-A

11531506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, undefined
orthologous variants: 148333794-G-T

http://identifiers.org/hco/1/GRCh38#11531508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#148333792-A-C

11531508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron_variant, undefined
orthologous variants: 148333792-A-T

11531655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148333650-G-T

11531711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: splice donor variant
orthologous variants: 148333594-G-A

http://identifiers.org/hco/1/GRCh38#11531725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148333581-C-A

11531725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148333581-C-T

11531737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148333579-C-T

http://identifiers.org/hco/1/GRCh38#11531765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148333549-C-A

http://identifiers.org/hco/1/GRCh38#11531780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148333533-C-A

11531780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148333533-C-T

11531808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148333506-T-C

11532292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148333232-C-T

http://identifiers.org/hco/1/GRCh38#11533618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148329349-C-A

11533618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329349-C-T

11533653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329315-G-C

11533653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329315-G-T

11533710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148329258-T-C

http://identifiers.org/hco/1/GRCh38#11533715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148329245-C-A

http://identifiers.org/hco/1/GRCh38#11533718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148329242-C-A

11533718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148329242-C-T

http://identifiers.org/hco/1/GRCh38#11533722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148329238-C-A

11533723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148329237-A-G

11533871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329112-G-A

11533871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329112-G-T

11533872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329111-G-T

11533873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329110-G-C

11533876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329107-T-A

11533876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329107-T-G

11533878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329105-G-T

11533889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329094-C-T

11533910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329074-T-G

11533913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329071-C-G

11533913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329071-C-T

http://identifiers.org/hco/1/GRCh38#11533918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148329065-C-A

11533936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329049-G-A

11533936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329049-G-T

11533940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329045-A-T

11533949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329036-G-A

11533949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329036-G-T

11533964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329010-G-A

11533964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329010-G-T

11533971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329003-G-C

11533974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148329000-A-G

http://identifiers.org/hco/1/GRCh38#11534071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148328907-C-A

11534090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328889-C-T

http://identifiers.org/hco/1/GRCh38#11534166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148328827-A-C

11534249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328784-G-A

11534249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328784-G-C

11534249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328784-G-T

11534384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148328717-A-G

http://identifiers.org/hco/1/GRCh38#11534552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148328549-C-A

11534552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328549-C-T

11534557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328545-C-T

11534576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328520-C-G

11534576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328520-C-T

11534613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328481-G-A

11534620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328470-G-T

http://identifiers.org/hco/1/GRCh38#11534669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148328421-C-A

11534669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328421-C-G

11534669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328421-C-T

11534674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328416-G-A

11534674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328416-G-T

11534678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328410-G-A

11534678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328410-G-T

11534724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328364-A-G

11534734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328354-G-A

11534734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328354-G-T

11534783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328308-G-A

11534783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328308-G-T

11534927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328040-G-T

http://identifiers.org/hco/1/GRCh38#11534953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148328017-C-A

11534953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148328017-C-T

11534982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327932-G-T

http://identifiers.org/hco/1/GRCh38#11535002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148327908-C-A

11535002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327908-C-T

11535043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327867-T-A

11535043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327867-T-C

11535070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327840-G-A

11535070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327840-G-T

http://identifiers.org/hco/1/GRCh38#11535109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148327801-C-A

11535109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327801-C-T

http://identifiers.org/hco/1/GRCh38#11535185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148327672-C-A

11535185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327672-C-G

11535185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327672-C-T

11535216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327617-A-G

11535219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327614-T-A

11535219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327614-T-C

11535225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327608-T-A

11535245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327587-T-A

11535245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327587-T-G

11535337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327525-T-A

11535337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327525-T-C

http://identifiers.org/hco/1/GRCh38#11535340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148327522-C-A

11535340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327522-C-T

11535410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327447-A-T

11535414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327443-C-T

http://identifiers.org/hco/1/GRCh38#11535430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148327427-C-A

http://identifiers.org/hco/1/GRCh38#11535435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148327412-A-C

11535435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327412-A-G

11535436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327411-G-T

11535438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327409-G-A

11535438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327409-G-T

http://identifiers.org/hco/1/GRCh38#11535439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148327408-C-A

11535439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327408-C-T

11535543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327301-A-G

11535573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327271-G-A

11535573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148327271-G-C

11535657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327183-C-T

11535727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327126-A-G

11535733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148327120-A-G

11535870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: intron variant
orthologous variants: 148326984-G-A

11536360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148326037-G-T

11536363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148326034-G-A

11536363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148326034-G-T

11536372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148326025-G-A

11536372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148326025-G-T

11536375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148326022-G-T

11536396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148326001-G-T

11536408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148325989-G-A

11536447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148325950-C-G

11536540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148325857-G-A

http://identifiers.org/hco/1/GRCh38#11536610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325787-C-A

11536610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 148325787-C-T

11536615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148325782-G-A

11536615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: 148325782-G-T

http://identifiers.org/hco/1/GRCh38#11536642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325755-C-A

11536642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: missense_variant, stop_gained
orthologous variants: 148325755-C-T

11536664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148325733-T-C

11536669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148325728-G-A

11536669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148325728-G-T

11536672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148325725-G-A

11536672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 148325725-G-T

http://identifiers.org/hco/1/GRCh38#11536689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325708-C-A

11536689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325708-C-T

11536696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325701-G-T

11536697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325700-G-A

11536697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325700-G-T

11536710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325686-G-A

11536710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325686-G-T

11536756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325667-G-A

11536756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325667-G-C

11536756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325667-G-T

11536763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325660-G-T

http://identifiers.org/hco/1/GRCh38#11536829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325612-C-A

11536867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325602-T-A

11536867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325602-T-G

11536979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325516-G-T

http://identifiers.org/hco/1/GRCh38#11537020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325478-C-A

11537020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325478-C-T

http://identifiers.org/hco/1/GRCh38#11537024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325474-C-A

11537050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325448-G-T

11537095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325405-G-A

11537095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325405-G-T

11537101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325399-G-A

11537101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325399-G-C

11537101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325399-G-T

11537153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325350-G-A

11537153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325350-G-C

11537153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325350-G-T

11537159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325345-G-A

11537159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325345-G-T

11537183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325321-T-A

11537183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325321-T-C

11537183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325321-T-G

http://identifiers.org/hco/1/GRCh38#11537190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325314-A-C

11537190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325314-A-G

11537194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325310-T-A

11537194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325310-T-C

11537194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325310-T-G

http://identifiers.org/hco/1/GRCh38#11537235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148325296-C-A

11537316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325232-A-G

11537326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325224-T-C

11537361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29251
most severe consequence: 3 prime UTR variant
orthologous variants: 148325189-T-C