132571720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66251681-C-T

132571810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66251771-T-C

132571855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66251816-C-T

132571918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66251878-G-T

132572154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66252099-G-C

132572154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66252099-G-T

132572279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66252216-C-T

132572303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 66252240-G-A

132572385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66252325-C-T

132572435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66252375-T-C

132572471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66252411-G-A

132572478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 66252418-C-T

132572576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252515-G-A

http://identifiers.org/hco/8/GRCh38#132572578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66252517-C-A

132572703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252627-T-A

132572703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252627-T-C

132572703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252627-T-G

132572801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252700-C-T

132573087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66252924-T-C

132573292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66253097-A-G

132573366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66253150-G-T

132573805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66253581-T-C

132573810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66253586-C-T

132573920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66253691-C-T

132574918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260211-A-G

132574930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260218-C-T

132575280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260392-G-T

132575423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260516-T-A

132575423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260516-T-G

132575428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260521-G-A

132575444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260537-T-C

132575562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66260652-T-A

132579114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66261996-T-C

http://identifiers.org/hco/8/GRCh38#132580287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66265493-A-C

http://identifiers.org/hco/8/GRCh38#132580359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66265549-C-A

132580658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66265800-A-G

132580761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66265896-G-A

132581493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66266489-T-C

http://identifiers.org/hco/8/GRCh38#132581987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66267040-C-A

132582064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66267116-C-T

132582071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66267123-C-T

132582145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66267197-G-A

132582274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66267563-C-T

132582750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66267994-T-C

132582794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268037-C-T

132582836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268080-T-A

132582979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268215-T-C

132583557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268694-A-G

132583574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268711-T-C

132583638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268775-A-T

132583646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268783-T-C

132583656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268793-A-G

132583700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66268836-T-G

132583771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66268907-T-C

132583791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268927-A-G

132583797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268933-C-T

132583809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268945-G-A

132583809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268945-G-T

http://identifiers.org/hco/8/GRCh38#132583844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66268984-C-A

132583844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66268984-C-T

132583849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269033-A-G

132583879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269071-A-T

http://identifiers.org/hco/8/GRCh38#132583891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66269085-C-A

132583891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269085-C-T

132584167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269337-G-A

132584236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269402-T-C

132584261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269427-G-A

132584305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269468-C-T

132584674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269847-C-T

132584725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269887-G-A

132584805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269948-C-T

132584859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66269990-C-T

132584920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270049-A-G

132584952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270080-A-G

132584995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270095-T-C

132586864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270298-T-C

132586965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270394-T-C

132587106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270518-G-A

132587451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270829-A-T

132587642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66270975-G-T

132587669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271002-T-C

132587976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271293-G-A

132587986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271303-G-A

132587986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271303-G-T

132588198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66271548-G-A

132588378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272434-T-C

132588607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66272648-C-T

132590736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275191-C-T

132590835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275295-T-C

132591184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275575-C-T

132591412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275795-C-G

132591537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275911-G-C

132591548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66275922-G-A

132591915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66276227-T-C

132592091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66276645-A-T

http://identifiers.org/hco/8/GRCh38#132592240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66276814-A-C

http://identifiers.org/hco/8/GRCh38#132592930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66277430-C-A

132593076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66277576-G-A

132593144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66277636-A-G

132593180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66277670-G-A

132593180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66277670-G-T

132596634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66296065-G-A

132596645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66296076-C-T

132602234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66296426-C-T

132602455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66296770-T-C

132602601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66296926-T-G

132603651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66300469-T-C

132603780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66300598-T-C

132603796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66300613-A-G

132603910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66300722-A-G

132604446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66301163-C-T

132604563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66301283-G-C

132604571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66301291-T-C

132604950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66301662-T-C

http://identifiers.org/hco/8/GRCh38#132604990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66302482-A-C

132605100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66302612-G-A

132607504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66303626-G-A

132607786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66304843-T-C

132607786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66304843-T-G

132607789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66304846-G-A

132607834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66304871-T-C

132608095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66305124-T-C

132608271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66305306-T-C

132608469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66305472-A-T

132608470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66305473-A-G

132608555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 66305678-T-A

132608555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 66305678-T-C

132608555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 66305678-T-G

132608569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66305691-A-G

http://identifiers.org/hco/8/GRCh38#132608573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66305695-C-A

http://identifiers.org/hco/8/GRCh38#132608611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66305730-C-A

132608611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66305730-C-T

132608615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66305734-T-A

132608696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66305826-G-T

132609990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309277-G-A

http://identifiers.org/hco/8/GRCh38#132610014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66309294-C-A

132610123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309401-C-G

http://identifiers.org/hco/8/GRCh38#132610356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66309629-C-A

132610356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309629-C-T

132610418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309691-G-A

132610483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309756-A-T

132610655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309925-C-G

132610745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66309997-A-G

132610749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310001-G-A

132610749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310001-G-T

132611429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310351-T-C

132611430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310352-A-G

132611434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310356-T-C

132611481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310403-G-A

http://identifiers.org/hco/8/GRCh38#132611568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66310488-C-A

132611568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310488-C-G

132611568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310488-C-T

132611733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310658-A-G

132611989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310843-T-C

132612058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310896-G-A

132612070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66310908-C-T

132612214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311061-G-A

132612539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311354-A-G

http://identifiers.org/hco/8/GRCh38#132612584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66311408-C-A

132612584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311408-C-G

132612636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311463-C-G

132612756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311586-C-T

132612757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311587-G-A

132612797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311624-A-G

132612806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311633-A-G

132613023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 66311774-A-G

132613105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66311833-C-T

132613118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66311846-G-A

132613226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311937-G-C

132613228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66311939-G-C

132613325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312031-A-G

132613461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312163-T-C

132613483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312185-T-A

132613483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312185-T-C

132613655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312327-G-T

132613856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312545-G-A

132614043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312692-T-C

132614354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312946-G-A

132614362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66312954-C-G

132614679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313264-G-A

132614679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313264-G-T

132614720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313432-A-T

132614761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313505-G-A

132614781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313525-C-T

132614810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313554-T-C

http://identifiers.org/hco/8/GRCh38#132614955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66313888-C-A

http://identifiers.org/hco/8/GRCh38#132614968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66313935-C-A

132614968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313935-C-T

132615009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313976-A-G

132615021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313989-G-A

132615021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66313989-G-T

http://identifiers.org/hco/8/GRCh38#132615110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66314085-C-A

132615122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314114-A-G

132615123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314115-A-G

132615218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314229-A-G

132615224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314235-G-T

132615234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66314245-A-G

http://identifiers.org/hco/8/GRCh38#132615237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66314248-C-A

132619533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316797-G-A

132619660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66316940-G-A

132619808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317086-G-T

132619880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317158-T-G

132619903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317177-G-A

132620011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317251-T-G

132620087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317328-C-G

http://identifiers.org/hco/8/GRCh38#132620395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66317479-C-A

132620395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317479-C-T

132620608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317524-T-C

132620745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317634-G-A

132620746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317635-G-C

132620774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317666-T-G

132620887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317759-G-C

132620982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317801-T-C

132621039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66317859-G-C

132621217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318026-C-T

132621528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318328-T-C

132621530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318330-G-A

132621693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318486-G-A

132621717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318507-T-G

132621719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318509-A-T

132621860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318617-A-G

132621880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318637-G-A

132622142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66318918-A-G

132622221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319072-G-A

132622460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319310-G-T

132622474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319324-T-C

http://identifiers.org/hco/8/GRCh38#132622513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66319361-A-C

http://identifiers.org/hco/8/GRCh38#132622671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66319503-A-C

132622718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66319557-G-A

132622718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66319557-G-C

132622718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66319557-G-T

132622775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66319605-G-C

132622775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66319605-G-T

http://identifiers.org/hco/8/GRCh38#132622793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66319651-A-C

132622793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66319651-A-T

http://identifiers.org/hco/8/GRCh38#132622794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66319652-A-C

132622907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66319759-T-C

132623160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320004-T-C

132623318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320157-T-C

http://identifiers.org/hco/8/GRCh38#132623373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66320300-A-C

132623752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66320635-G-T

132625158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321177-T-C

132625164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321183-T-A

132625177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321199-G-T

http://identifiers.org/hco/8/GRCh38#132625182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66321204-A-C

132625182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321204-A-T

132625231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321251-A-G

http://identifiers.org/hco/8/GRCh38#132625267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66321287-A-C

132625430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66321456-G-A

132625440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66321466-C-T

http://identifiers.org/hco/8/GRCh38#132625442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66321468-C-A

132625442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66321468-C-T

132625483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321518-A-T

http://identifiers.org/hco/8/GRCh38#132625571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66321604-C-A

132625571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321604-C-G

132625656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321647-A-G

132625740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321723-C-G

132625814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66321782-G-C

132627171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322693-T-C

132627180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66322702-C-T

132627320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66323935-A-G

132627332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66323947-A-G

132627406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324012-A-T

132627693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324293-A-G

132627818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324408-T-C

132627968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324501-T-C

132628010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324543-C-T

132628083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66324618-C-T

http://identifiers.org/hco/8/GRCh38#132628090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66324625-C-A

132632068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325253-C-T

132632081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325266-T-C

132632123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325308-C-G

132632128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325313-A-G

132632245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325422-C-T

132632472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325636-G-A

http://identifiers.org/hco/8/GRCh38#132632593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66325783-C-A

132632593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66325783-C-T

http://identifiers.org/hco/8/GRCh38#132632783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66325961-C-A

132632783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66325961-C-T

http://identifiers.org/hco/8/GRCh38#132632788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66325966-C-A

132632906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66326087-A-G

http://identifiers.org/hco/8/GRCh38#132632928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66326109-C-A

132632928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66326109-C-T

132633105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326415-C-T

132633325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66326622-A-G

132633533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66333668-T-C

132633828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66333958-C-G

http://identifiers.org/hco/8/GRCh38#132633864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66333994-C-A

132633874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334004-G-A

132633874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334004-G-C

132633977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334128-C-T

132634095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334236-T-C

132634106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334247-T-C

http://identifiers.org/hco/8/GRCh38#132634178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66334303-C-A

132634420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334576-A-G

132634431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334594-T-C

132634486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334630-T-A

132634518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334663-G-A

132634581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334726-T-A

132634814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334864-T-C

132634841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334884-C-T

132634962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66334998-T-C

132634988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335020-T-C

132635448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335503-G-T

132635529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335574-T-C

132635530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335575-G-A

132635534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335579-A-G

132635570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335615-T-G

132635849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335774-G-T

132635970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66335914-C-T

132636146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336107-C-T

132636148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336109-T-C

132636429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336429-T-A

132636429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336429-T-C

132636450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336450-C-T

132636475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336473-T-G

132636620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336602-G-A

http://identifiers.org/hco/8/GRCh38#132636710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66336698-C-A

132636710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336698-C-G

132636710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336698-C-T

132636842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336826-T-G

132636959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336933-G-T

132637009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66336984-T-C

http://identifiers.org/hco/8/GRCh38#132637105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66337111-A-C

132637821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341526-G-A

132637821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341526-G-T

132637844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341549-C-T

132637857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341567-G-A

132637857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341567-G-T

132637900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341610-T-C

132637914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66341636-G-A

132637983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66341714-G-C

132638040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66341771-G-A

132639341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66342130-G-A

132639368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66342151-C-T

132639506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66342259-G-A

132640863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66342679-C-T

132641056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66342822-G-T

132641163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66342926-G-T

132641425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66343178-G-A

132641442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66343195-C-T

132641493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66343246-G-C

132641801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66344051-C-T

http://identifiers.org/hco/8/GRCh38#132641835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66344086-A-C

132642008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66344246-T-C

132642063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66344289-G-A

132650842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66347035-A-G

132651020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66347222-G-C

132651081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66347272-A-G

132651233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66347389-A-G

http://identifiers.org/hco/8/GRCh38#132651265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66347421-C-A

http://identifiers.org/hco/8/GRCh38#132651285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66347449-A-C

132651372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66347599-G-A

132651584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66347860-G-A

132651740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66348007-C-T

132651853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66348120-C-T

132652034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66348279-G-T

132652206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66348445-C-T

132652539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66348740-A-G

132655958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352250-T-C

132656028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352322-T-C

132656031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352325-A-G

132656102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352389-T-A

132656102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352389-T-C

132656130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352416-A-G

132656153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352439-A-T

132656371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66352945-C-G

132656818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353078-A-G

132656941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353195-A-G

132656966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353215-G-A

132656966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353215-G-T

http://identifiers.org/hco/8/GRCh38#132657049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66353707-C-A

132657166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353820-G-A

132657246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353887-T-C

132657343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353980-G-A

132657343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66353980-G-C

132657509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66354140-A-G

132657681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66354289-T-C

132657750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66354354-T-C

132658353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66356921-C-T

132658359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66356927-G-A

132658467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357023-C-T

132658468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357024-G-A

132658485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357042-G-A

132658644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357194-A-T

132658682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357240-C-T

http://identifiers.org/hco/8/GRCh38#132658760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66357319-C-A

132658760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357319-C-T

132658792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357347-T-C

132658793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357348-G-C

132658915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357457-T-C

132659144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66357694-A-G

132659553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358104-C-T

132659605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358156-A-G

132659828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358366-G-A

132659830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358368-G-A

132659916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358463-T-C

132659988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358550-C-T

132660158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358694-C-T

132660408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358847-C-T

132660418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358857-G-A

132660487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66358927-G-T

132660499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66358939-C-T

132660516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66358960-T-C

132660516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66358960-T-G

http://identifiers.org/hco/8/GRCh38#132660579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66359022-C-A

132660629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66359066-G-C

132660629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66359066-G-T

132660702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66359143-C-T

132660733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66359210-C-G

132660879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66359343-T-G

132660920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66359383-A-T

132661064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66360183-G-A

http://identifiers.org/hco/8/GRCh38#132661319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66361194-C-A

132661340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361215-G-A

132661340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361215-G-T

132661357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361230-G-A

132661357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361230-G-T

132661437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361291-G-A

132661704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361566-G-A

132661704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361566-G-C

132661704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361566-G-T

132661796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361661-G-T

132661800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361665-T-C

132661846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361714-T-C

132661891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361759-G-A

132661976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361844-G-A

132661976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361844-G-C

132662027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66361890-G-A

132662240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66362007-T-C

132662411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66362165-T-C

132662514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66362272-T-A

132662605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66362367-C-T

132662641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66362403-A-T

132662734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66363829-T-C

132663051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364129-C-G

132663057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364135-T-C

132663135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364198-C-G

132663150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364213-A-T

132663188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364252-C-T

132663221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364270-G-A

132663264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364327-G-C

132663405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364634-C-T

132663780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66364998-T-C

132663842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365060-A-G

132663856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365072-G-A

132663883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365099-G-A

132663891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365107-G-C

132664122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365346-T-C

http://identifiers.org/hco/8/GRCh38#132664130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66365350-C-A

132664130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365350-C-G

132664258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365481-T-C

132664287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365510-C-G

132664343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365563-C-T

132664422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66365626-G-A

132665150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66366464-G-A

132667559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66367328-C-T

132667566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66367335-A-T

132667622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66367415-A-G

132667751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66367535-C-G

132668933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66368867-G-A

132669049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66368967-A-G

132669255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66369151-G-A

132669255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66369151-G-T

132669330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66369231-G-A

132669553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66369442-G-A

132670142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66369945-A-G

132670451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66370311-C-T

132670512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66370368-T-A

132670512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66370368-T-C

132670579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66370430-A-G

132675317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 66372518-C-T

132675342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372542-G-A

132675342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372542-G-C

132675342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372542-G-T

132675354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372554-G-A

132675354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372554-G-C

132675354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372554-G-T

http://identifiers.org/hco/8/GRCh38#132675360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66372560-A-C

132675360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66372560-A-G

132675497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372637-G-A

132675497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372637-G-C

132675497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372637-G-T

132675526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372666-G-A

132675526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372666-G-C

132675526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372666-G-T

http://identifiers.org/hco/8/GRCh38#132675538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#66372678-C-A

132675538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372678-C-G

132675538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372678-C-T

http://identifiers.org/hco/8/GRCh38#132675547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#66372687-C-A

132675547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372687-C-G

132675547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372687-C-T

132675566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372706-G-A

132675566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372706-G-C

132675566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372706-G-T

http://identifiers.org/hco/8/GRCh38#132675567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#66372707-C-A

132675567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372707-C-G

132675567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372707-C-T

132675603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372743-G-A

132675603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372743-G-T

http://identifiers.org/hco/8/GRCh38#132675628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66372768-C-A

132675628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66372768-C-T

http://identifiers.org/hco/8/GRCh38#132675641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#66372781-C-A

132675641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372781-C-G

132675641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372781-C-T

132675663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 66372803-G-C

132676181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66373372-C-T

132676710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66373883-A-G

132677157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66374354-T-C

132677422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66374650-T-G

132679436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66375681-A-G