124984411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132585131-T-A

124984411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132585131-T-G

http://identifiers.org/hco/10/GRCh38#124984453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132585172-C-A

124984453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132585172-C-G

124984453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132585172-C-T

http://identifiers.org/hco/10/GRCh38#124984544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132585250-C-A

124984602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132585297-A-G

http://identifiers.org/hco/10/GRCh38#124984626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132585327-A-C

124984626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132585327-A-G

124984927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 132585615-C-T

124984983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 132585671-A-T

http://identifiers.org/hco/10/GRCh38#124985007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132585696-C-A

124985007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132585696-C-T

http://identifiers.org/hco/10/GRCh38#124985010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132585699-C-A

124985010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132585699-C-T

http://identifiers.org/hco/10/GRCh38#124985072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132585761-C-A

124985072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132585761-C-T

124985144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132585828-T-C

124985144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132585828-T-G

124985209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132585895-A-T

http://identifiers.org/hco/10/GRCh38#124985260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132585997-C-A

124985260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132585997-C-T

124985540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132586279-G-C

124985540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132586279-G-T

124985610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132586379-G-T

124985743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132586501-G-T

124986796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132587472-T-C

124986796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132587472-T-G

124986933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132587606-G-T

http://identifiers.org/hco/10/GRCh38#124986953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132587624-C-A

http://identifiers.org/hco/10/GRCh38#124987092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132587776-A-C

124987110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132587800-G-A

124987460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588153-C-T

124987643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588264-T-C

124987781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588365-G-A

124987781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588365-G-C

124987781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588365-G-T

http://identifiers.org/hco/10/GRCh38#124988100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132588557-C-A

124988203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588623-G-T

124988242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588653-T-C

124988257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588668-T-C

124988267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588677-A-G

124988306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132588710-T-C

http://identifiers.org/hco/10/GRCh38#124988560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132588969-C-A

124988790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 132589199-C-T

124988899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 132589325-G-A

124988899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 132589325-G-T

124988902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 132589350-T-C

124989170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132589581-T-C

124989205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132589616-T-C

http://identifiers.org/hco/10/GRCh38#124989389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132589796-C-A

http://identifiers.org/hco/10/GRCh38#124989433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132589834-C-A

124989495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3 prime UTR variant
orthologous variants: 132589877-T-C

124989527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: synonymous variant
orthologous variants: 132589909-G-A

124989527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: missense variant
orthologous variants: 132589909-G-C

124989527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: missense variant
orthologous variants: 132589909-G-T

124989680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: synonymous variant
orthologous variants: 132590062-C-T

http://identifiers.org/hco/10/GRCh38#124992643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132591674-C-A

124992643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591674-C-T

124992654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591681-T-A

124992654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591681-T-C

124992654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591681-T-G

http://identifiers.org/hco/10/GRCh38#124992851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132591873-C-A

124992851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591873-C-T

124992915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591957-A-G

124992933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591983-G-A

124992933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132591983-G-T

http://identifiers.org/hco/10/GRCh38#124992958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132592026-C-A

124992958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132592026-C-T

124992987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron variant
orthologous variants: 132592056-C-T

124993376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592336-G-A

http://identifiers.org/hco/10/GRCh38#124993394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132592346-C-A

124993398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592350-A-G

124993435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592390-A-G

124993781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592692-G-A

124993781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592692-G-C

124993781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592692-G-T

124993812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592722-T-C

124993884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 132592797-G-C

124993908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 132592821-C-T

124994053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592974-A-G

124994053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592974-A-T

http://identifiers.org/hco/10/GRCh38#124994055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132592976-A-C

http://identifiers.org/hco/10/GRCh38#124994064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132592985-C-A

124994064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132592985-C-T

124994080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593006-T-G

124994088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593014-G-A

124994088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593014-G-T

124994178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593104-A-G

http://identifiers.org/hco/10/GRCh38#124994346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132593205-C-A

124994346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593205-C-G

124994346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593205-C-T

124994408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593227-C-T

124994535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 132593357-G-A

124994541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, stop_gained, synonymous_variant
orthologous variants: 132593363-G-A

http://identifiers.org/hco/10/GRCh38#124994689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132593511-C-A

124994689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 132593511-C-G

124994689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 132593511-C-T

124994739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593559-G-A

124994800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593618-G-A

124994800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593618-G-C

http://identifiers.org/hco/10/GRCh38#124994813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132593628-C-A

124994813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593628-C-G

124994813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132593628-C-T

124995705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132594950-T-G

http://identifiers.org/hco/10/GRCh38#124995711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132594956-A-C

124995735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132594988-C-T

124995746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132594999-T-C

124995822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 132595084-A-T

124996777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132595976-T-C

http://identifiers.org/hco/10/GRCh38#124996778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132595977-C-A

124996798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132595999-T-C

124996817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596018-G-T

124996821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596023-G-A

124996821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596023-G-C

124996821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596023-G-T

124996862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596055-A-G

http://identifiers.org/hco/10/GRCh38#124996880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596074-A-C

124996880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596074-A-G

http://identifiers.org/hco/10/GRCh38#124996884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596079-C-A

124996908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596104-A-G

124997011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596184-A-G

124997057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596203-G-A

124997057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596203-G-T

124997122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596261-G-C

124997122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596261-G-T

124997151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596290-A-T

124997226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596359-G-A

124997226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596359-G-C

124997226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596359-G-T

124997262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596395-G-A

124997262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596395-G-C

http://identifiers.org/hco/10/GRCh38#124997351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596426-A-C

124997351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596426-A-G

http://identifiers.org/hco/10/GRCh38#124997358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596433-C-A

124997358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596433-C-T

124997399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596468-G-A

124997455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596537-C-G

124997562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596638-G-A

124997562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596638-G-C

124997582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596650-G-A

124997582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596650-G-T

http://identifiers.org/hco/10/GRCh38#124997585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596653-A-C

124997681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596737-A-G

124997716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596768-G-A

124997726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596776-A-T

http://identifiers.org/hco/10/GRCh38#124997728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596778-A-C

124997728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596778-A-G

124997777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596828-G-A

124997777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596828-G-C

124997777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596828-G-T

http://identifiers.org/hco/10/GRCh38#124997914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596865-C-A

124997914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596865-C-T

124997960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596884-G-A

124997960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596884-G-C

124997960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132596884-G-T

124998022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132596946-G-A

124998022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132596946-G-T

124998031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132596955-C-T

http://identifiers.org/hco/10/GRCh38#124998049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132596973-C-A

124998049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132596973-C-T

124998079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132597003-C-G

124998079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132597003-C-T

124998169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 132597093-T-C

124999556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132598001-G-A

124999556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132598001-G-T

124999663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132598097-G-A

124999663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132598097-G-C

124999663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132598097-G-T

124999806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132598219-T-C

http://identifiers.org/hco/10/GRCh38#124999824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132598227-A-C

124999828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132598231-T-C

125001389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132599274-C-T

http://identifiers.org/hco/10/GRCh38#125001399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132599280-C-A

125001399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132599280-C-T

125002961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 132600537-G-A

125002961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 132600537-G-C

125003236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132600845-G-A

125003272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132600881-G-C

125003272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132600881-G-T

http://identifiers.org/hco/10/GRCh38#125003497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132601079-C-A

125003522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132601111-G-T

125003523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132601112-G-T

125005847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132603473-A-G

125005925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132603560-A-G

125005926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132603561-T-C

http://identifiers.org/hco/10/GRCh38#125006092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132603724-C-A

125006092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132603724-C-G

125006388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132603907-T-C

125006485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132603990-A-G

125006486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132603991-C-G

http://identifiers.org/hco/10/GRCh38#125006601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132604030-A-C

125006707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604109-G-A

125006750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604136-G-A

125006780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604188-C-T

125006930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604326-C-G

125006930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604326-C-T

125006931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604327-C-T

125007168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604496-C-T

125007170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604498-G-A

125007198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604526-A-G

125007288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132604617-G-A

125007772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132605209-C-T

125007865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132605297-G-A

125012070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132607093-G-A

125012071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132607094-A-G

125012312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132607296-G-T

125012317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132607301-G-A

125013181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132607865-T-C

125013288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132607987-C-T

125013425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132608103-C-T

125013448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132608126-G-A

http://identifiers.org/hco/10/GRCh38#125013478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132608148-C-A

125014926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609434-C-T

125014955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609472-G-A

125014959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609476-G-A

125015037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609541-C-T

125015074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609583-A-G

125015085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609593-C-T

125015091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609599-G-T

125015110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609611-G-A

125015110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609611-G-T

125015423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609840-G-A

125015530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132609943-G-A

125016007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610369-C-T

125016155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610471-T-C

125016236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610550-C-T

125016241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610555-T-C

125016252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610566-T-C

125016374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610639-C-T

http://identifiers.org/hco/10/GRCh38#125016483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132610737-A-C

125016585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610832-G-A

125016608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610847-T-A

125016647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610894-G-C

125016647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610894-G-T

125016669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132610913-G-C

125017223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132611270-G-A

125017233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132611280-G-A

125017233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132611280-G-C

125017317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132611360-T-C

125017474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132611515-C-T

125017520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132611557-C-T

125023444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612384-T-C

125023446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612386-G-A

125023491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612409-G-A

125023571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612479-T-C

http://identifiers.org/hco/10/GRCh38#125023883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132612704-A-C

125023966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612794-C-G

125023966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612794-C-T

125023990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132612822-G-A

125024136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613030-A-G

125024259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613148-A-G

125024373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613261-G-A

125024373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613261-G-C

125024509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613397-G-A

125024530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613418-G-T

125024545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613428-G-C

125024878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132613764-G-C

125025065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614140-T-C

125025070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614145-G-A

125025092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614170-T-C

125025109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614187-C-T

125025141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614230-T-A

125025141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614230-T-G

125025145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614234-G-A

125025341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614414-G-A

125025572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614637-C-T

125025660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614732-C-G

125025705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614776-G-T

125025741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614807-G-A

125025741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614807-G-C

125025741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614807-G-T

125025743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614809-G-A

125025807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614872-T-C

125025952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614991-T-G

125025957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132614996-T-C

125025964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615026-G-A

125025964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615026-G-T

125026005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615179-T-C

http://identifiers.org/hco/10/GRCh38#125026019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132615193-C-A

125026019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615193-C-T

125026038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615212-T-C

125026054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615225-G-A

125026054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615225-G-T

125026067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132615238-G-A

125026125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132615290-T-A

125026125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132615290-T-C

125026125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132615290-T-G

http://identifiers.org/hco/10/GRCh38#125026131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132615296-C-A

125026131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132615296-C-T

http://identifiers.org/hco/10/GRCh38#125026257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132615425-C-A

125026257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132615425-C-T

http://identifiers.org/hco/10/GRCh38#125026295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#132615463-C-A

125026295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132615463-C-G

125026295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132615463-C-T

125026394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132615565-G-A

125026394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132615565-G-T

125026449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132615620-G-A

125026449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132615620-G-C

125026484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132615655-C-T

http://identifiers.org/hco/10/GRCh38#125026565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132615736-C-A

125026565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132615736-C-T

125026597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132615789-G-A

125026875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616067-G-C

125026875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616067-G-T

125026941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616133-G-A

125026941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 132616133-G-C

125026941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 132616133-G-T

125026978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132616170-C-T

125027097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616289-A-T

125027191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132616389-C-T

125027232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616430-C-T

125027263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132616461-C-T

125027343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616541-G-A

125027406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616604-A-G

125027529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132616727-G-A

125027539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132616737-G-A

125027539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132616737-G-C

125027590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132616770-G-C

125027653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132616836-C-T

http://identifiers.org/hco/10/GRCh38#125027661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132616844-C-A

125027829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132617004-A-G

http://identifiers.org/hco/10/GRCh38#125027853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132617028-A-C

125027991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132617164-A-G

125028022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132617196-G-A

125028022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132617196-G-C

125028093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617269-G-A

http://identifiers.org/hco/10/GRCh38#125028184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132617359-C-A

125028473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132617610-T-C

http://identifiers.org/hco/10/GRCh38#125028572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132617707-C-A

125029891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132619874-C-G

125029894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132619877-G-C

125030350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620464-G-A

125030363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620477-G-T

http://identifiers.org/hco/10/GRCh38#125030515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132620589-C-A

125030515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620589-C-T

125030658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620685-G-A

http://identifiers.org/hco/10/GRCh38#125030789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132620810-A-C

125030802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620823-G-C

125030802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132620823-G-T

http://identifiers.org/hco/10/GRCh38#125030847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132620876-C-A

http://identifiers.org/hco/10/GRCh38#125030934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132620962-A-C

125031023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132621032-C-T

125033824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622161-G-C

125034596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132622827-G-A

125034831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623026-T-C

125034958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623098-C-G

125034993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623130-G-A

125035015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623165-G-A

125035323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132623356-T-C

125035347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623380-G-A

125035347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132623380-G-T

125035457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132623455-C-G

125036100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624079-C-T

125036120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624099-C-T

125036126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624105-G-C

125036303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132624316-C-T

125037562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132625955-C-T

http://identifiers.org/hco/10/GRCh38#125037721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132626120-C-A

125037721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626120-C-T

125037742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626136-T-G

125037938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626380-T-C

125037951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626393-T-C

125038014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626487-T-A

125038212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132626693-T-C

125038878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132627299-T-C

125039247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627693-G-T

125039387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132627845-G-A

125040567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132628589-A-G

http://identifiers.org/hco/10/GRCh38#125040629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132628680-A-C

125041651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629256-C-T

125041749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629342-G-C

125041749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629342-G-T

125041788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629373-G-A

125041826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629411-T-C

125042185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629696-T-C

125042299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132629817-G-A

125043110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132630966-G-A

125043175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631015-A-G

125044455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631710-A-T

125044520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631766-T-C

125044545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132631791-T-C

125046924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132632988-C-T

125047425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633477-A-T

125047471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633560-C-T

125047600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132633698-C-G

125047786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634017-G-A

125047859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634086-A-G

125048034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132634265-G-A

125048045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634276-T-C

125048122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634332-C-T

125048179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132634391-G-A

125048243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132634459-T-C

125048335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132634543-A-T

125048363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132634570-A-G

125048455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132634644-C-T

http://identifiers.org/hco/10/GRCh38#125048843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132635036-C-A

125048846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132635039-C-G

http://identifiers.org/hco/10/GRCh38#125048918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132635102-C-A

125054834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637246-C-T

125054850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637262-T-C

125054896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637303-C-G

125054902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637309-T-C

125054905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637312-G-A

125054973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637380-G-A

125054979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637386-C-G

125054979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637386-C-T

125055064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637471-A-G

125055303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637688-G-A

125055427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637865-C-T

125055428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132637866-G-A

125055847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132638262-C-T

125056964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132638807-C-T

125057925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132639651-C-T

125058086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132639784-G-C

125058319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132640018-G-C

125058414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132640121-T-C

125058797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132640527-G-A

125058875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132640594-C-T

http://identifiers.org/hco/10/GRCh38#125059078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132640853-C-A

125059141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132640947-G-A

http://identifiers.org/hco/10/GRCh38#125059201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132641034-C-A

125059201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132641034-C-T

125059869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132641497-G-C

125059893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132641521-G-C

125059902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132641529-T-C

125060311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132641894-T-C

125060640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642267-A-T

125060658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642285-C-T

125060683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642307-C-T

http://identifiers.org/hco/10/GRCh38#125060791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132642408-C-A

125060927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132642485-C-T

125061134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642683-G-A

125061246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132642831-T-A

125062980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644094-G-T

125063094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644184-G-C

125063135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644227-G-A

http://identifiers.org/hco/10/GRCh38#125063359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132644384-C-A

125063359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644384-C-T

125063581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644592-G-A

125063653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644665-G-A

125063782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644796-A-G

125063811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132644821-T-C

125064856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132646486-G-A

125066193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132647172-T-C

125066242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132647220-G-A

125066244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132647222-A-G

125066447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132647408-T-C

125066697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132647511-T-A

125066989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132647781-G-C

125068170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648567-A-T

125068218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132648616-C-T

http://identifiers.org/hco/10/GRCh38#125071342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132650080-C-A

125071494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650222-T-C

125071752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650458-T-C

125071859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650585-G-A

125072766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132650883-G-A

125073036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651162-C-G

125073074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651202-C-T

125073116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651243-C-T

125073149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651289-A-G

125073186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651314-T-C

125073508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651677-T-C

125073648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651800-C-T

125073663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651815-A-G

http://identifiers.org/hco/10/GRCh38#125073810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132651938-A-C

http://identifiers.org/hco/10/GRCh38#125073826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132651949-C-A

125073826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651949-C-T

125073899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132651994-C-T

125073920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652029-C-T

125074001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652110-C-T

125074129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652229-G-A

125074271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652361-G-A

125074340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132652436-T-C

125076625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654478-G-A

125076650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654494-G-A

125076720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654545-C-T

125076769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654574-T-A

125076792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654597-G-A

125076805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654609-T-C

125076854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654656-A-G

125077107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132654907-T-C

125077301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132655461-G-A

125077421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132655582-T-C

125077788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132655945-G-A

125077788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132655945-G-T

125077906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132656052-T-A

125078443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132656564-G-C

125078761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132656852-G-A

125079151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132657301-A-G

125079157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132657307-A-G

http://identifiers.org/hco/10/GRCh38#125079468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132657676-A-C

125079469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132657677-T-A

125079933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132658133-T-A

125079933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132658133-T-C

125080664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132658762-A-G

125082376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659535-G-A

125082376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659535-G-C

125082477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659624-T-A

125082488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659635-G-C

125082491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659638-T-C

125082491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659638-T-G

http://identifiers.org/hco/10/GRCh38#125082510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132659657-A-C

125082510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659657-A-T

http://identifiers.org/hco/10/GRCh38#125082513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132659660-C-A

http://identifiers.org/hco/10/GRCh38#125082515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132659662-C-A

125082518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659665-A-G

125082535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132659679-G-A

125084330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132660366-G-A

125084583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132660611-C-T

125084584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132660612-A-G

125084669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132660692-C-T

125084764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132660805-C-T

125084772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132660813-C-T

125084822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132660866-C-T

125085046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132661105-C-T

125085287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132661313-C-T

125085303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132661329-G-A

125085589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132661613-T-A

125085609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132661630-G-A

125085824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132661952-G-A

125085892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662010-G-A

125086020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662156-G-A

125086105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662239-T-C

http://identifiers.org/hco/10/GRCh38#125086181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132662314-A-C

125086207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662335-G-A

125086881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662884-G-A

125086881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662884-G-C

125086881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662884-G-T

125086896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662899-G-A

http://identifiers.org/hco/10/GRCh38#125086943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132662946-C-A

125086947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132662991-G-A

125089018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132664702-T-C

125089094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132664775-A-G

125089149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132664828-G-A

http://identifiers.org/hco/10/GRCh38#125089163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132664842-A-C

125089163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132664842-A-G

125089315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132665078-C-T

125089380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132665124-C-T

125089408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132665152-C-T

125092838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132667917-T-C

125093277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132668233-C-G

125093277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132668233-C-T

125093322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132668282-A-G

125093403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132668361-T-C

125093552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132668513-C-T

125093824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132668829-G-C

125093862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132668867-G-C

125094435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132669473-C-T

125094479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132669524-G-A

125094527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132669600-C-T

125094725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132669764-C-T

125094801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132669840-T-C

125096907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132670638-A-G

125097430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132671158-T-C

125097483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132671217-C-T

125097596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132671323-C-G

125097596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132671323-C-T

125097603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132671327-G-A

125097824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132671694-C-T

125099270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132672785-T-G

125099389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132672891-G-A

125099406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132672908-G-C

125099433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132672961-C-T

125099442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132672970-C-G

125099542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132673059-C-T

125099621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132673137-A-G

http://identifiers.org/hco/10/GRCh38#125100458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132673896-C-A

125100725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132674672-C-T

125100981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132674920-G-T

125101007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132674946-T-A

125101008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132674947-G-A

125101038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132674977-G-T

125101687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132675652-T-C

125101741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132675710-T-C

125101741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132675710-T-G

125102724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132676648-C-T

125102830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132676745-G-A

125102831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132676746-G-A

125102831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132676746-G-C

125102972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132676868-G-T

125104270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132677995-C-T

125104537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132678438-A-G

125104537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132678438-A-T

http://identifiers.org/hco/10/GRCh38#125105867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132679739-A-C

http://identifiers.org/hco/10/GRCh38#125105988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132679832-C-A

125105988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132679832-C-T

125106069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132679912-C-T

http://identifiers.org/hco/10/GRCh38#125106437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132680255-A-C

125106437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132680255-A-G

125106619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132680485-C-G

125106670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132680542-C-G

125106670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132680542-C-T

125106687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132680554-C-T

125107073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132680871-A-G

125107319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132681048-C-T

125107607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132681271-A-G

125107650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132681317-C-G

125109657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132682262-A-G

125109729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132682309-G-A

125109893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132682455-T-C

125110565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132683065-C-G

125111125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132683621-T-C

http://identifiers.org/hco/10/GRCh38#125111754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132684238-C-A

125111754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132684238-C-T

125113304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132685016-A-T

http://identifiers.org/hco/10/GRCh38#125113480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132685125-C-A

125113725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132685543-T-C

125113758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132685576-T-C

http://identifiers.org/hco/10/GRCh38#125113848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132685670-A-C

125113975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132685801-T-A

125113985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132685812-A-G

125114027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132685852-T-A

125114073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132685898-G-C

125114198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686022-G-A

125114198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686022-G-C

125114198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686022-G-T

http://identifiers.org/hco/10/GRCh38#125117466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132686353-C-A

125117466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686353-C-T

125117545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686429-G-A

125117614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686484-G-A

125117727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686604-C-T

125118047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686912-G-A

125118047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686912-G-C

125118060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132686925-G-A

125118420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132687233-G-A

125118420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132687233-G-C

125122461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689637-G-C

125122614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689786-G-A

125122614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689786-G-T

125122615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689787-T-A

125123627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690276-T-C

125123739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690359-C-G

125123739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690359-C-T

125124174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690751-C-T

125124306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690886-C-T

125124393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690973-C-T

125124497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691086-G-A

125124506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691094-T-C

125124998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691626-C-G

125125073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691716-C-T

125125185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691828-A-G

125125522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692128-G-A

125130681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132695801-A-G

125130878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132695985-G-A

125131094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696201-C-T

125132292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696352-G-A

125132293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696353-G-A

125132309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696365-C-T

125132396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696445-T-A

125132535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696578-C-G

125132694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696717-T-A

125132694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132696717-T-C

http://identifiers.org/hco/10/GRCh38#125133073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132697051-A-C

http://identifiers.org/hco/10/GRCh38#125133074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132697052-A-C

http://identifiers.org/hco/10/GRCh38#125133187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132697535-C-A

125133187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697535-C-G

125133347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697672-C-T

125133372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697696-A-G

125133372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697696-A-T

125133390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697714-G-A

125133390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697714-G-T

125133468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697782-T-C

http://identifiers.org/hco/10/GRCh38#125133531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132697847-C-A

125133531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132697847-C-T

125133551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132697867-A-T

125133627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697912-T-C

125133635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132697920-T-C

125133743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132698015-C-T

125135575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132699357-C-T

125135592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132699375-C-T

125135881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132699671-T-C

125135925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132699717-G-A

125136045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132699797-T-C

http://identifiers.org/hco/10/GRCh38#125136050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132699802-A-C

125136177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132699914-G-A

125136201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132699929-G-C

125136606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132700242-T-A

125136629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132700265-C-T

125136809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132700434-C-T

125137065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132700645-C-T

125137416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701154-C-T

125137764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701512-A-G

125137859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701606-G-T

125137864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701611-G-A

125137865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132701612-G-A

125140421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132703840-C-T

125140422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132703841-G-A

125140499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132703912-C-T

http://identifiers.org/hco/10/GRCh38#125140626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132703993-C-A

http://identifiers.org/hco/10/GRCh38#125141418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132704150-C-A

125141998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704463-G-A

125141998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704463-G-T

125142111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704594-C-T

125142203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704665-G-A

125142289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704744-T-A

125142477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705002-T-G

125142520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705093-T-A

125142750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705302-G-C

125142905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705408-G-A

125142905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705408-G-C

125142924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705427-A-G

125142945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705436-G-A

125142995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705491-C-T

125143028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705526-T-G

http://identifiers.org/hco/10/GRCh38#125143228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132705833-C-A

125143228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132705833-C-G

125143954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708096-C-G

125144090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708214-A-G

125144689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709895-G-T

125144787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710037-G-A

125144842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710120-C-G

125144908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710192-G-A

125144908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710192-G-T

125145009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710314-G-A

125145091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132710392-G-C

125145517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132710806-G-A

125146834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711679-C-T

125147052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711898-C-G

125147072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711917-C-T

125147655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712443-T-A

125147932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712613-T-C

125148042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712710-G-A

125148536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713236-T-C

125148570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713271-T-C

http://identifiers.org/hco/10/GRCh38#125149116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132713837-C-A

125149149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713861-G-C

125149663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132714313-A-G

125150015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132714641-G-C

http://identifiers.org/hco/10/GRCh38#125150041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132714666-A-C

125151954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716825-A-G

125152005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716866-C-T

125152032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716889-A-G

http://identifiers.org/hco/10/GRCh38#125152293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132717023-C-A

125152446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132717180-C-G

125152446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132717180-C-T

http://identifiers.org/hco/10/GRCh38#125152850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132717540-A-C

125152868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132717562-T-G

125153037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132717726-G-A

125153225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132717935-G-A

125153688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718236-G-C

125153784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718317-C-T

http://identifiers.org/hco/10/GRCh38#125153850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132718384-A-C

125153950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718435-C-T

125154370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718889-T-C

125154387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718906-G-A

125154387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718906-G-T

125154424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718943-G-A

125154547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132719066-G-A

125154547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132719066-G-C

125154854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132719342-T-C

125155383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132719847-T-C

125155706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132720165-T-A

125155807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132720263-G-A

125156390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132720792-T-G

125156427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132720830-T-A

125156450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132720853-G-C

125156551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132720978-G-T

125157013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132721626-A-G

125157265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132721926-G-A

125157359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132722046-G-A

125157373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132722064-G-A

125158159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132722816-T-A

125158587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132723215-C-T

http://identifiers.org/hco/10/GRCh38#125158596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132723224-A-C

125158809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132723419-G-T

125159031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132723631-G-A

125159110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132723710-G-A

125159110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132723710-G-C

125159231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132723825-G-C

125159552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724110-G-A

125159645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724203-G-A

http://identifiers.org/hco/10/GRCh38#125159711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132724270-C-A

125159711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724270-C-G

125159711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724270-C-T

http://identifiers.org/hco/10/GRCh38#125159714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132724273-C-A

125159736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724295-G-A

125159736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724295-G-T

125159879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132724436-G-A

125159879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132724436-G-C

125160088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 132724649-G-A

125160088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 132724649-G-T

125160100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132724661-G-A

125160100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132724661-G-T

http://identifiers.org/hco/10/GRCh38#125160115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132724676-C-A

125160287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724835-C-G

125160287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132724835-C-T

http://identifiers.org/hco/10/GRCh38#125160303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132724851-C-A

http://identifiers.org/hco/10/GRCh38#125160423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#132724977-C-A

125160423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132724977-C-G

125160423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132724977-C-T

125160643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132725198-T-A

125160643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132725198-T-C

125160643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132725198-T-G

125161030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132725596-T-G

125161038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132725602-G-A

125161051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132725615-T-C

125161053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132725628-C-T

125161077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132725644-G-A

125161077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2495
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132725644-G-T