151494164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4432586-T-C

http://identifiers.org/hco/6/GRCh38#151494167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4432589-C-A

151494167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4432589-C-T

151494183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, splice_region_variant, undefined
orthologous variants: 4432598-G-A

151494183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: splice_region_variant, stop_gained, undefined
orthologous variants: 4432598-G-T

151494192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 4432604-T-A

151494192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 4432604-T-C

http://identifiers.org/hco/6/GRCh38#151494210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#4432622-C-A

151494210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4432622-C-T

151494255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4432668-G-A

151494255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4432668-G-C

151494311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4432712-G-T

151494894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4433070-C-T

151495121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4433230-C-G

151495188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4433288-A-G

151496485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4434681-G-C

151496607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4434785-T-G

151498001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4435738-G-A

151498001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4435738-G-T

151498060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4435798-T-C

151501258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4437468-T-G

151501337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4437591-A-G

151501409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4437753-T-C

151501741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4438387-G-A

http://identifiers.org/hco/6/GRCh38#151501971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4438616-C-A

http://identifiers.org/hco/6/GRCh38#151502739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4439414-C-A

151504177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4439869-T-C

151504230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4439920-T-G

151504257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4439948-C-T

151504583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4440241-A-G

http://identifiers.org/hco/6/GRCh38#151504584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4440242-C-A

151509522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4442433-A-G

151512934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4444388-A-G

151513018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4444470-T-A

151523151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4452159-G-T

151523154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4452162-T-G

151523162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4452170-T-A

151523186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4452195-G-C

151523707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4452404-G-T

151527361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4456887-T-C

151527377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4456903-C-G

151527760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4457643-C-T

151527770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4457653-T-C

151527808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4457691-A-G

151527953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4457842-C-T

151528020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4457909-G-T

151528096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4457984-A-G

http://identifiers.org/hco/6/GRCh38#151528230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4458118-A-C

151528230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4458118-A-G

151528397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4458576-A-G

151528456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4458630-G-A

http://identifiers.org/hco/6/GRCh38#151528476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4458650-C-A

151534489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4460337-T-C

151534706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4460548-G-T

http://identifiers.org/hco/6/GRCh38#151534799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4460646-C-A

151534799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4460646-C-T

151534832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4460682-G-A

151535590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4461296-G-A

http://identifiers.org/hco/6/GRCh38#151535605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4461307-C-A

151535605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4461307-C-G

151536156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4462594-T-C

151536179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4462619-A-G

151536331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4462765-A-G

http://identifiers.org/hco/6/GRCh38#151536333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4462767-C-A

151536333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4462767-C-G

http://identifiers.org/hco/6/GRCh38#151536354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4462788-C-A

151536354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4462788-C-T

151536355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4462789-G-A

151536355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4462789-G-C

http://identifiers.org/hco/6/GRCh38#151536368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4462802-C-A

151536440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4462874-G-A

151536477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4462913-T-G

151536834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4462960-G-A

151537033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4463099-C-T

151537424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4463412-C-T

151538103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4464114-C-G

151538103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4464114-C-T

151538104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4464115-T-C

151538128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4464139-C-T

151539482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4465700-G-A

http://identifiers.org/hco/6/GRCh38#151539657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4465817-A-C

151539718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4465833-A-G

151540108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4466144-G-A

151540108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4466144-G-T

151540220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4466252-G-C

151540220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4466252-G-T

151540275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4466302-C-G

151542637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4467660-T-C

151542829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4467853-C-T

151544161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4468498-G-C

http://identifiers.org/hco/6/GRCh38#151544455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4468789-C-A

151544455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4468789-C-T

151544462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4468796-G-A

http://identifiers.org/hco/6/GRCh38#151544503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4468837-C-A

151544506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4468840-A-G

151544674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4469008-T-G

151544690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4469024-G-A

151544698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4469032-T-G

151544769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469102-T-C

151544769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469102-T-G

151544775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469108-G-A

151544775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469108-G-T

151544785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469118-G-T

151544797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469130-T-A

151544797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469130-T-C

151544875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469605-C-T

151544882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469612-G-C

151547403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469926-G-A

151547433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4469956-G-T

151547484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470015-G-A

151547525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470051-G-A

http://identifiers.org/hco/6/GRCh38#151547526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4470052-A-C

151547626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470127-C-G

151547915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470365-T-C

151547922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470372-C-T

http://identifiers.org/hco/6/GRCh38#151548178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4470613-C-A

151548247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470675-G-C

151548248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470676-A-T

151548289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470740-T-C

151548493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4470944-T-C

151549220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4471133-A-G

151549229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4471142-G-T

151549310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4471243-A-G

151549871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4472097-A-T

151550053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4472626-G-T

151553207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4474581-C-G

151553219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4474594-G-A

151553354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4474722-G-A

151553423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4474786-T-A

151553474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4474814-G-T

151568965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4479673-G-T

151569047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4479741-T-C

151569201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4479893-T-A

151569219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4479911-G-A

151569219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4479911-G-T

151569454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4480771-T-C

151569491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4480801-A-G

151569596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4480909-G-A

151570084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4481530-T-A

151570209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4481655-T-C

151570517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4481991-A-T

151570546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482033-T-C

151570566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482092-G-A

151570627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482141-T-C

151570674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482185-C-T

151570757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482271-T-G

151570952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482440-C-T

151571058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482536-A-T

151571091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482582-T-C

151571231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4482719-G-A

151573038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4483842-G-T

151573071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4483877-T-A

151573071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4483877-T-C

151573108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4483911-T-C

151573143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4483932-G-A

151573143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4483932-G-T

http://identifiers.org/hco/6/GRCh38#151573153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4483942-C-A

151573237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4484022-A-G

151573248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4484033-T-A

151573248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4484033-T-G

151573345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4484130-G-C

151573390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4484175-G-A

151573390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4484175-G-C

151573428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4484213-C-G

151573428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4484213-C-T

http://identifiers.org/hco/6/GRCh38#151573437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4484222-C-A

151573476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4484261-A-G

151576715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4487627-A-G

151576932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4487831-C-T

151576979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4487882-T-C

151576983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4487886-T-C

151579817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4489113-T-A

151584413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4489965-T-A

151584492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490048-C-T

151584559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490120-A-T

151584596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490156-G-A

151584634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490207-A-G

151585056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490615-A-G

151585089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490648-G-A

151585133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490693-T-A

151585147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4490713-A-G

151585792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4491587-A-G

http://identifiers.org/hco/6/GRCh38#151585811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4491605-C-A

151585892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, missense_variant
orthologous variants: 4491685-G-A

151586012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, missense_variant
orthologous variants: 4491805-G-C

151586012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, missense_variant
orthologous variants: 4491805-G-T

151586117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4491909-T-A

151586117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4491909-T-C

151586165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4491955-T-C

151586165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4491955-T-G

151586206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4491989-T-A

151586727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4492473-A-G

151587506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4493062-C-T

151587598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4493153-T-A

151590457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4493989-C-T

http://identifiers.org/hco/6/GRCh38#151590600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4494108-C-A

http://identifiers.org/hco/6/GRCh38#151590601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4494111-A-C

151590652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4494162-T-A

151590652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4494162-T-C

151590665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4494175-T-C

http://identifiers.org/hco/6/GRCh38#151590729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4494620-C-A

http://identifiers.org/hco/6/GRCh38#151590735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4494626-C-A

151590743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4494634-T-C

151590892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4495180-C-T

151591329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4495617-T-G

151591343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4495624-C-T

151592911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4496604-G-A

151592911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4496604-G-T

http://identifiers.org/hco/6/GRCh38#151592931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4496624-C-A

151592931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4496624-C-T

151593020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4496685-G-A

151593056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4496721-T-C

151593258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4496917-T-C

151593417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4497069-G-T

http://identifiers.org/hco/6/GRCh38#151593428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4497080-A-C

151593428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4497080-A-G

151594133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4497529-A-G

151594150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4497546-A-G

151594270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4497724-C-G

151594405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4497851-G-A

151594560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4498031-A-G

151594616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4498086-C-T

http://identifiers.org/hco/6/GRCh38#151594673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4498119-C-A

151594673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4498119-C-T

151595238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4498781-C-G

151595470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4498989-T-A

151596031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4499240-G-A

151596320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4499542-T-A

151596320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4499542-T-G

151596442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4499664-G-C

151596448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4499670-G-C

151596454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4499676-C-T

http://identifiers.org/hco/6/GRCh38#151596470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4499692-A-C

151596610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4499831-T-C

151603276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502072-A-T

http://identifiers.org/hco/6/GRCh38#151603282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4502078-A-C

151603282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502078-A-G

151603448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502237-G-A

151603502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502292-A-G

151603775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502707-G-T

151603870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502801-C-T

151603994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502916-G-C

151604063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4502975-C-T

151604243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4503149-G-A

151609297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4503604-C-T

http://identifiers.org/hco/6/GRCh38#151609363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4503660-A-C

151609521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4503813-G-T

151609658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4503950-C-T

151609659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4503951-G-A

151609712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4504003-C-T

151609726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4504017-A-G

151609746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4504037-G-A

151609746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4504037-G-T

151610775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4504542-C-T

151610896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4504652-T-A

151610896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4504652-T-C

151611013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4504770-G-A

151611013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4504770-G-T

151614088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4507049-A-G

http://identifiers.org/hco/6/GRCh38#151614134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4507092-C-A

151614443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4507390-T-G

http://identifiers.org/hco/6/GRCh38#151615022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4508115-A-C

151615304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4508361-C-T

151615327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4508384-T-C

151615330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4508387-T-C

151615418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4508472-T-C

151615420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4508474-T-C

http://identifiers.org/hco/6/GRCh38#151615576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4508630-C-A

151615669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4508723-G-T

http://identifiers.org/hco/6/GRCh38#151615805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4508827-C-A

151615805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4508827-C-G

151615805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4508827-C-T

151615846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4508867-C-T

151615911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4508931-A-T

151616446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4509457-T-A

151616541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4509550-G-T

151616544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4509553-C-T

151616618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4509629-T-A

151616638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4509649-G-T

151616841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4509807-C-T

151616974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4509928-T-A

151617110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510072-A-G

http://identifiers.org/hco/6/GRCh38#151617162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4510123-C-A

151617219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510174-T-C

151617421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510423-T-G

151617446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510448-T-A

151617456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510458-T-C

151617456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510458-T-G

151617498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510481-C-T

151617568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron variant
orthologous variants: 4510542-C-G

151617800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4510746-A-T

151617839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4510785-C-T

151617853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4510799-G-C

151617853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4510799-G-T

151617865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4510806-G-C

151617865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: intron_variant, undefined
orthologous variants: 4510806-G-T

151617976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4510928-G-C

151617979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4510931-G-A

151618004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4510956-G-C

151618004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4510956-G-T

151618030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4510982-G-A

151618141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4511105-T-G

151618144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4511108-T-A

151618144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: synonymous variant
orthologous variants: 4511108-T-C

151618144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: missense variant
orthologous variants: 4511108-T-G

http://identifiers.org/hco/6/GRCh38#151618211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4511180-C-A

151618211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511180-C-T

151618325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511522-G-A

151618325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511522-G-T

151618397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511590-T-G

151618444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511639-T-A

151618444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511639-T-C

151618488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511676-T-C

151618488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4511676-T-G

http://identifiers.org/hco/6/GRCh38#151619139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4512300-C-A

151619145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4512306-G-T

151619219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4512542-T-C

http://identifiers.org/hco/6/GRCh38#151619258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#4512581-C-A

151619268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4512591-G-T

151619303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4512982-C-T

151619327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4513007-C-T

151619367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4513041-T-C

151620849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4514074-A-G

151620852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4514077-C-T

151620887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21177
most severe consequence: 3 prime UTR variant
orthologous variants: 4514112-T-C