192576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138740839-G-A

192653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138740913-C-T

192725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138740975-C-T

192824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741051-C-T

http://identifiers.org/hco/7/GRCh38#192830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138741057-C-A

192884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741117-C-T

http://identifiers.org/hco/7/GRCh38#192892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
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/5/GRCm39#138741125-C-A

192892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138741125-C-T

192910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138741147-G-A

http://identifiers.org/hco/7/GRCh38#193004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138741194-C-A

193004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741194-C-G

193004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741194-C-T

http://identifiers.org/hco/7/GRCh38#193019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138741209-A-C

193019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741209-A-G

193019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741209-A-T

http://identifiers.org/hco/7/GRCh38#193022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138741212-C-A

193046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 138741236-G-A

http://identifiers.org/hco/7/GRCh38#193054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138741244-C-A

193054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741244-C-G

http://identifiers.org/hco/7/GRCh38#193174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138741367-C-A

193174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741367-C-T

http://identifiers.org/hco/7/GRCh38#193305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138741496-C-A

193305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741496-C-T

193402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741593-G-A

193402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138741593-G-T

193631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 138741807-C-T

193823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742019-G-A

193823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742019-G-C

193823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742019-G-T

193854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742072-G-A

193854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742072-G-T

193919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742120-G-A

193919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742120-G-C

193919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742120-G-T

193920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742121-T-A

193920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742121-T-C

193924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742125-G-T

http://identifiers.org/hco/7/GRCh38#194194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138742412-A-C

194194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742412-A-G

194214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742431-G-A

194214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742431-G-T

194239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742456-G-A

194239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742456-G-C

194239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742456-G-T

http://identifiers.org/hco/7/GRCh38#194253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138742470-A-C

194253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742470-A-G

http://identifiers.org/hco/7/GRCh38#194291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138742499-A-C

194291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742499-A-G

http://identifiers.org/hco/7/GRCh38#194399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138742560-A-C

194399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138742560-A-T

194972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743007-G-A

194991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743026-T-C

195038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138743075-C-T

195092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743130-G-A

195092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743130-G-T

195140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743177-G-C

195140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743177-G-T

195178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743196-G-A

195178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743196-G-T

195183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743201-G-A

195183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743201-G-T

195186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743204-A-G

http://identifiers.org/hco/7/GRCh38#195195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138743212-C-A

195195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743212-C-T

195251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743272-G-A

195251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743272-G-T

195290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743302-T-G

195316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138743328-T-C

195493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743493-G-A

195493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743493-G-C

195493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138743493-G-T

195696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138743698-C-G

196076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744033-C-T

196670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744485-C-T

196747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744556-T-C

196747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138744556-T-G

198602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746070-C-T

198792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746193-T-C

198843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746243-C-T

199253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746536-C-T

199266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746549-G-C

199390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746681-G-A

199390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746681-G-T

199426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138746717-C-T

199479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747191-G-A

199550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747265-T-A

199574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747289-C-T

199759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747474-T-G

199881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747609-G-A

199881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747609-G-T

200035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747768-A-G

200041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747774-C-T

200091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138747822-C-T

200435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748065-G-A

200435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138748065-G-C

http://identifiers.org/hco/7/GRCh38#200911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138748482-C-A

200911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748482-C-T

200976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748554-C-T

201003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748580-G-A

201039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748614-T-G

201092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748654-C-G

201092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748654-C-T

201316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138748896-G-A

203770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138749922-A-G

203796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138749948-G-A

203958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750095-G-A

204049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138750185-T-C

208547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138752028-T-G

208754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138752219-A-G

http://identifiers.org/hco/7/GRCh38#208848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138752327-A-C

208855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138752334-T-C

http://identifiers.org/hco/7/GRCh38#208891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138752377-C-A

208891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138752377-C-T

209025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138752504-G-A

209027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138752506-G-A

209027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138752506-G-C

211814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138755520-G-A

211917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138755614-C-T

211933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138755630-G-A

212096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138755759-G-T

220181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138762532-C-G

222370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763527-G-A

222370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763527-G-C

222504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763635-G-A

222667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763732-C-G

222667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763732-C-T

222837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138763882-G-A

222959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138764020-C-T

223025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138764109-G-A

226928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765676-C-G

226936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765684-T-C

227160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765828-A-G

227203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765877-G-A

227242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765893-G-A

227321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765976-A-G

227340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138765995-C-T

227488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138766174-A-G

http://identifiers.org/hco/7/GRCh38#229257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138768631-A-C

229257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768631-A-G

229257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768631-A-T

229264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768638-T-G

229286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768662-G-A

229286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768662-G-T

http://identifiers.org/hco/7/GRCh38#229306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138768682-A-C

http://identifiers.org/hco/7/GRCh38#229431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138768785-C-A

229431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768785-C-T

229459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768808-A-G

229459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768808-A-T

229462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768811-G-T

229465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768814-C-T

229489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768836-C-T

229535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768866-G-T

http://identifiers.org/hco/7/GRCh38#229539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138768870-C-A

229540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138768871-A-G

229595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138768922-G-A

229636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138768934-A-G

229647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138768945-A-G

229654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138768952-A-G

229654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138768952-A-T

229661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138768959-G-A

229732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138769037-G-A

233794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138770501-G-A

235477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138771623-T-C

235716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138771866-C-T

235780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138771917-C-G

235780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138771917-C-T

235791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138771938-T-C

235948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772131-G-A

235948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772131-G-T

235968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772152-T-C

236149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772292-G-A

http://identifiers.org/hco/7/GRCh38#236171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138772314-C-A

236217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138772358-G-A

236966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774325-C-G

236966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138774325-C-T

http://identifiers.org/hco/7/GRCh38#246193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138777259-C-A

246201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138777267-G-A

246201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138777267-G-T

246204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138777272-G-A

246204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138777272-G-T

http://identifiers.org/hco/7/GRCh38#246209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138777277-C-A

246209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138777277-C-T

246214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138777282-G-T

246276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138777330-C-T

246369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138778896-G-A

246369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138778896-G-T

246436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138778963-A-G

246439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138778966-C-G

246525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779042-C-T

246967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779425-A-T

247125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779538-G-A

247125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779538-G-C

247135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779548-A-G

247291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779671-C-G

247291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779671-C-T

247543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138779868-G-A

248068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780540-G-T

http://identifiers.org/hco/7/GRCh38#248069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138780541-C-A

http://identifiers.org/hco/7/GRCh38#248189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138780654-C-A

248200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780665-G-A

248200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138780665-G-T

248438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138780872-G-A

248438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138780872-G-T

253661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138788652-G-A

253661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138788652-G-C

254061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138789054-A-G

254070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138789063-G-A

255925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138792038-G-A

255964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138792077-C-G

255964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138792077-C-T

http://identifiers.org/hco/7/GRCh38#255982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792095-C-A

255982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138792095-C-G

255982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138792095-C-T

256046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792167-G-A

256070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792191-G-A

256070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792191-G-C

256076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792197-G-A

256117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792247-G-A

256117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792247-G-T

256127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792257-G-T

256165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792328-G-A

256165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138792328-G-T

http://identifiers.org/hco/7/GRCh38#256196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792395-C-A

256196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792395-C-T

http://identifiers.org/hco/7/GRCh38#256206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792414-C-A

256206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792414-C-T

256209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792417-T-A

256209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792417-T-C

256209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792417-T-G

256275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792474-G-A

256275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792474-G-T

256291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792489-G-A

256291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792489-G-C

256291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792489-G-T

http://identifiers.org/hco/7/GRCh38#256438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792736-C-A

256438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792736-C-G

256438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792736-C-T

256550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792839-A-G

256567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792853-G-A

256567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792853-G-T

256592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792884-G-A

256592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792884-G-T

http://identifiers.org/hco/7/GRCh38#256596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792891-C-A

256596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792891-C-T

http://identifiers.org/hco/7/GRCh38#256598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792893-C-A

256598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792893-C-T

http://identifiers.org/hco/7/GRCh38#256627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792933-C-A

256627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792933-C-T

http://identifiers.org/hco/7/GRCh38#256640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138792977-C-A

256640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138792977-C-G

256663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138793015-G-A

256699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138793051-G-A

256699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138793051-G-T

http://identifiers.org/hco/7/GRCh38#256767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138793119-C-A

256767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793119-C-T

256888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793144-C-T

256929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793180-C-G

256978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793208-T-C

257009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138793233-C-T

http://identifiers.org/hco/7/GRCh38#257016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138793240-C-A

257016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138793240-C-G

257016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138793240-C-T

257066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138793290-C-G

257066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138793290-C-T

http://identifiers.org/hco/7/GRCh38#257108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138793330-C-A

257108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138793330-C-T

257112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138793334-C-T

http://identifiers.org/hco/7/GRCh38#257113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138793335-C-A

257113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138793335-C-G

257120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138793342-A-T

http://identifiers.org/hco/7/GRCh38#258741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138793870-C-A

258741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793870-C-T

258841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793951-T-A

258841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793951-T-C

258841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138793951-T-G

258998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794059-C-G

259025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794085-C-T

259079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794142-C-G

259151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794212-G-A

259151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794212-G-T

259223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794304-T-A

259244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794333-C-T

http://identifiers.org/hco/7/GRCh38#259502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138794643-C-A

http://identifiers.org/hco/7/GRCh38#259514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138794655-C-A

259514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794655-C-T

http://identifiers.org/hco/7/GRCh38#259528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138794669-C-A

259528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794669-C-G

259528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794669-C-T

259530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794671-G-A

259530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794671-G-C

259530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794671-G-T

http://identifiers.org/hco/7/GRCh38#259564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138794706-C-A

259564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794706-C-G

259592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794735-T-A

259592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794735-T-C

259592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794735-T-G

259593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794736-T-C

259595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794738-T-A

259595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794738-T-C

http://identifiers.org/hco/7/GRCh38#259618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138794761-C-A

259618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794761-C-G

259618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794761-C-T

259627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794770-T-A

259627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794770-T-C

259627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794770-T-G

259631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794774-T-A

259631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794774-T-C

259644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794788-T-C

http://identifiers.org/hco/7/GRCh38#259716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138794847-C-A

259716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794847-C-G

259716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138794847-C-T

259724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138794855-T-A

http://identifiers.org/hco/7/GRCh38#259759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138794891-C-A

259759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 138794891-C-T

259851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138794983-C-G

259887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138795019-A-G

259898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138795030-G-A

259898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138795030-G-T

260082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795181-G-A

260082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795181-G-C

260082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795181-G-T

260093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795192-G-A

http://identifiers.org/hco/7/GRCh38#260112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#138795213-C-A

260112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795213-C-T

260183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795288-A-T

260345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795418-G-A

260345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795418-G-T

260518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795563-G-A

260518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795563-G-T

260550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795597-T-A

260550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795597-T-C

260561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795608-C-T

260615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138795686-A-G

260747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22140
most severe consequence: 3 prime UTR variant
orthologous variants: 138795820-G-T