178513286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156936040-A-G

http://identifiers.org/hco/1/GRCh38#178513365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156935965-C-A

http://identifiers.org/hco/1/GRCh38#178513559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156935806-A-C

178513742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935656-T-A

178513808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935619-G-C

178513872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935557-G-A

http://identifiers.org/hco/1/GRCh38#178513895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156935541-C-A

178513967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935510-A-T

178514132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 156935359-G-T

http://identifiers.org/hco/1/GRCh38#178514232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156935256-C-A

178514232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935256-C-G

178514259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935224-C-G

178514452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935066-G-T

178514464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935054-C-T

178514498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156935010-C-T

178514568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156934955-G-A

http://identifiers.org/hco/1/GRCh38#178514634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156934890-C-A

178514754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 156934772-A-G

178515795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156932721-T-C

178515830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156932690-T-A

178515969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156932548-A-G

178516285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156932268-T-C

178516414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156932172-T-G

178516434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156932152-T-C

http://identifiers.org/hco/1/GRCh38#178516712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156931877-A-C

178516712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156931877-A-G

178516723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156931869-T-C

178516723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156931869-T-G

178516756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156931838-G-C

178516796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156931820-G-A

178516796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156931820-G-T

http://identifiers.org/hco/1/GRCh38#178517146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156931479-A-C

178517146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156931479-A-G

178517771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156930583-C-G

http://identifiers.org/hco/1/GRCh38#178517825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156930529-C-A

178518035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156930357-T-A

178518283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156929956-G-A

178518283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156929956-G-C

178518283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156929956-G-T

http://identifiers.org/hco/1/GRCh38#178518329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156929894-C-A

178518802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156929462-G-A

178519069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156929239-A-T

178519482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928906-G-T

178519915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928526-T-G

178520112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928337-A-G

178520142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928307-A-G

http://identifiers.org/hco/1/GRCh38#178520235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156928226-C-A

178520235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928226-C-T

178520321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928150-T-C

178520321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928150-T-G

178520329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928143-G-A

178520471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156928007-T-C

178520584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156927899-T-C

178520902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 156927620-A-G

http://identifiers.org/hco/1/GRCh38#178520943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156927580-C-A

178520943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156927580-C-T

http://identifiers.org/hco/1/GRCh38#178521018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156927520-C-A

178521018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156927520-C-G

http://identifiers.org/hco/1/GRCh38#178521046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156927492-C-A

http://identifiers.org/hco/1/GRCh38#178521069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156927469-C-A

178521082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156927459-G-A

178521357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156927176-C-T

178521601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 156926931-G-C

178521602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 156926930-C-T

178521760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926769-C-T

178521848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926675-T-C

178521849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926674-G-T

178521924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926557-T-C

178521978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926518-T-C

178522024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926473-G-T

178522043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926454-G-T

http://identifiers.org/hco/1/GRCh38#178522055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156926444-C-A

178522055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926444-C-T

178522057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926442-G-A

178522057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926442-G-T

http://identifiers.org/hco/1/GRCh38#178522127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156926379-A-C

http://identifiers.org/hco/1/GRCh38#178522160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156926346-C-A

178522160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926346-C-G

178522160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926346-C-T

178522175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926332-T-C

http://identifiers.org/hco/1/GRCh38#178522210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156926293-C-A

178522266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926264-T-C

http://identifiers.org/hco/1/GRCh38#178522313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156926215-C-A

178522313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926215-C-G

178522313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156926215-C-T

http://identifiers.org/hco/1/GRCh38#178522315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156926213-A-C

178523550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156925567-T-A

178523550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156925567-T-C

178523574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156925543-A-G

178523574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156925543-A-T

178523863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156925307-G-A

http://identifiers.org/hco/1/GRCh38#178525828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156922695-C-A

178525883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156922651-G-A

178525886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156922648-A-T

178525977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156922561-C-G

178526005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156922532-G-A

178526040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156922499-G-A

178526407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156922151-G-T

178527328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156921490-T-C

178527352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156921467-G-T

http://identifiers.org/hco/1/GRCh38#178527442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#156921374-C-A

http://identifiers.org/hco/1/GRCh38#178527469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#156921347-C-A

178527469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156921347-C-T

178527472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156921344-A-G

178527493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156921323-C-T

178527681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156920746-C-T

178527749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156920683-T-C

178527782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156920651-C-T

178527814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156920619-C-T

178528722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156919690-G-T

178528888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156919525-T-G

178530038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156918712-T-C

178530049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156918703-C-T

178530051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156918701-C-T

178530117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 156918636-A-T

178530157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156918598-G-C

178530157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156918598-G-T

178530207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156918549-A-T

178530241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156918505-C-T

178531584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914633-G-C

178531584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914633-G-T

178531667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914554-G-T

178531805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914427-G-A

178531805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914427-G-T

178531833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914414-G-A

178531833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914414-G-T

178531891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914391-T-C

178532029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914279-C-T

178532145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914166-G-A

178532301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914063-T-G

178532306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156914058-G-T

178532456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156913917-G-C

178532493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156913869-G-A

178532521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156913841-A-G

http://identifiers.org/hco/1/GRCh38#178532661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#156913729-C-A

178532697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156913699-C-T

178532818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156913588-G-A

178532961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 156913455-A-G

178533052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 156913363-T-C

178533931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156913023-T-C

http://identifiers.org/hco/1/GRCh38#178534192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156912505-C-A

178534201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156912497-A-G

178534274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156912414-C-T

178534377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156912312-A-T

http://identifiers.org/hco/1/GRCh38#178534591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156912100-C-A

178535833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156910218-C-T

178535922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156910128-G-A

178535922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156910128-G-T

178536141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156909910-T-A

178536773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156909242-G-A

178536828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156909188-T-C

178536889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156909157-T-C

http://identifiers.org/hco/1/GRCh38#178537252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156908803-C-A

178537331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908733-G-A

178537446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908646-G-T

http://identifiers.org/hco/1/GRCh38#178537459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156908633-C-A

178537459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908633-C-T

178537702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908489-C-T

178537737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908451-C-T

178537747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908441-A-G

178537922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908295-G-A

178538059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908139-C-T

178538089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908056-G-A

178538097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156908048-C-G

178538139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156907995-G-T

http://identifiers.org/hco/1/GRCh38#178538438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156907729-C-A

178538450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156907717-G-A

178538499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156907670-T-C

178538545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156907631-G-A

178538703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156907492-A-G

178538979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156907222-G-T

178538985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156907216-G-A

http://identifiers.org/hco/1/GRCh38#178539060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156907139-C-A

http://identifiers.org/hco/1/GRCh38#178539307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156906913-C-A

178539375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906841-A-T

178539474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906766-G-C

178539559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906701-C-T

178539695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906543-G-A

178539764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906479-G-A

178540248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906332-A-G

http://identifiers.org/hco/1/GRCh38#178540312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156906260-A-C

178540312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906260-A-G

178540342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906231-C-T

178540371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156906208-A-G

178540660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156905991-C-G

178540800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156905775-C-T

178541139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156905411-T-C

178541203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156905346-G-A

178541203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156905346-G-C

178541211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156905343-C-T

178544413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156903000-G-C

178544413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156903000-G-T

178544415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902998-T-C

178544512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902909-C-T

178544544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902878-C-T

178544888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902566-T-C

178544909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902546-C-T

178544912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902543-A-G

178544940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902516-A-G

178544968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902487-G-A

178544968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902487-G-C

178544972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902483-A-G

178545007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902448-T-G

178545008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902447-G-A

178545008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902447-G-C

178545055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902387-C-T

178545120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902320-G-A

178545187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902230-G-C

178545194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902223-C-T

178545216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156902201-G-T

178545576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156901415-G-A

178545705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156901293-T-G

178545867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156901062-A-G

http://identifiers.org/hco/1/GRCh38#178545875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#156901054-C-A

http://identifiers.org/hco/1/GRCh38#178546008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#156900899-A-C

178546008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156900899-A-G

178546008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156900899-A-T

178546012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156900895-T-A

178546012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156900895-T-C

178546012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156900895-T-G

178546016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156900893-T-C

http://identifiers.org/hco/1/GRCh38#178546055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#156900855-C-A

178548170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156899363-G-A

178548248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156899286-G-T

178548252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156899282-C-T

178548298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25366
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 156899237-G-T