173888451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31821018-G-A

173888451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31821018-G-C

173888451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31821018-G-T

http://identifiers.org/hco/5/GRCh38#173888826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31821393-C-A

173888826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5 prime UTR variant
orthologous variants: 31821393-C-G

173888826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5 prime UTR variant
orthologous variants: 31821393-C-T

173889105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5 prime UTR variant
orthologous variants: 31821671-G-T

173889538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5 prime UTR variant
orthologous variants: 31822102-A-G

173890180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: synonymous variant
orthologous variants: 31822734-T-G

173890908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31823462-G-A

173890908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31823462-G-C

173890928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31823482-G-C

173890928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31823482-G-T

http://identifiers.org/hco/5/GRCh38#173890987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31823536-C-A

173890987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31823536-C-G

http://identifiers.org/hco/5/GRCh38#173890988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31823537-C-A

173891387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31823879-A-G

173892477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31824972-A-G

173892477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31824972-A-T

http://identifiers.org/hco/5/GRCh38#173895170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31827124-A-C

173895334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31827289-T-G

173895367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31827314-C-T

173895792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31827844-G-A

173895799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31827851-T-C

173895926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31828227-C-T

173895994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31828295-G-A

173896156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31828458-A-G

173898758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31830633-C-T

173899375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31831229-T-C

173899465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31831303-A-G

173899852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31831637-A-G

173900037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31831784-C-T

173900988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31833013-G-A

http://identifiers.org/hco/5/GRCh38#173901703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31833669-A-C

173901764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31833728-A-G

173901779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31833743-G-A

173901807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31833771-T-C

173901958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31833900-A-G

http://identifiers.org/hco/5/GRCh38#173902703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31834572-C-A

173902942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31834824-T-C

http://identifiers.org/hco/5/GRCh38#173903041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31834927-A-C

173903079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31834957-T-A

173903079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31834957-T-C

http://identifiers.org/hco/5/GRCh38#173903132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31835002-A-C

173903270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31835131-G-T

173904596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31835913-A-G

173904760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31836054-T-C

173905540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31836794-C-T

http://identifiers.org/hco/5/GRCh38#173906279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31837350-C-A

173906293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31837364-C-T

173906412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31837472-G-A

173906620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31837704-T-C

173906704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31837790-C-G

173906742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31837826-G-T

173908566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31838144-A-T

173910132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31839460-C-G

173910170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31839498-C-G

173910900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31840203-G-A

173910921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31840222-A-T

173910935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31840228-A-G

173911830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31840680-G-A

173911830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31840680-G-C

173911974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31840854-T-A

173912429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31841294-T-C

173913546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31841581-A-G

173913825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31841832-G-C

173915018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31843179-G-A

173915045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31843205-T-C

http://identifiers.org/hco/5/GRCh38#173915146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31843303-C-A

173915146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31843303-C-T

173915289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31843453-C-T

http://identifiers.org/hco/5/GRCh38#173915582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31843936-C-A

173915582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31843936-C-G

173915759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31844082-G-A

173915862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31844173-C-G

173916290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31844632-G-A

173916417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, undefined
orthologous variants: 31844748-T-C

173916516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31844835-A-G

173916599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31844917-T-G

173916609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron_variant, undefined
orthologous variants: 31844927-T-C

173917214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31845504-A-G

173917257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31845542-G-A

173917754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31845782-A-G

173918217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31846225-G-C

173918241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31846248-G-T

173918266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31846275-T-C

173918266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31846275-T-G

173918284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31846295-G-A

173918500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31846471-C-T

173918654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31846620-T-A

173918963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31846927-G-A

173919001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31846957-T-C

173919048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31847005-A-G

173919123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31847082-C-T

173919440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31847412-A-G

173919451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31847423-G-A

173919583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31847567-C-G

173919643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31847633-T-C

173919769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31847751-G-A

http://identifiers.org/hco/5/GRCh38#173919952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31848207-A-C

173920417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31848619-T-G

173920471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31848673-G-C

173921392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31849830-A-G

173921712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850036-G-A

173921731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850054-G-A

173921862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850158-G-A

173921914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850215-T-C

173922131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850433-G-A

173923637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850709-G-A

173923698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850774-A-G

173923698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850774-A-T

173923774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31850845-G-A

173924558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31851563-A-G

173924858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31851850-G-T

173925165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31852524-G-A

173925335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31852664-G-A

http://identifiers.org/hco/5/GRCh38#173925455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31852776-A-C

173925971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31853240-A-G

173926482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31853731-G-A

173927449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855509-T-G

http://identifiers.org/hco/5/GRCh38#173927460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31855512-A-C

173927460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855512-A-G

173927841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855636-G-A

173927870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855665-A-G

173927956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855734-A-G

173927966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855739-A-G

173928064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855848-T-C

http://identifiers.org/hco/5/GRCh38#173928200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31855983-A-C

173928200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31855983-A-T

173928561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31856209-C-T

http://identifiers.org/hco/5/GRCh38#173928691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31856327-C-A

173928691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31856327-C-T

173929331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31856908-G-A

http://identifiers.org/hco/5/GRCh38#173929857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31857113-A-C

173929857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31857113-A-G

173930384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31857290-A-G

173930392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31857298-G-A

173931594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31858067-G-A

173931731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31858198-G-C

173932361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31858737-G-T

http://identifiers.org/hco/5/GRCh38#173932623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31859017-C-A

173932623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31859017-C-G

http://identifiers.org/hco/5/GRCh38#173932683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31859079-A-C

173933326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31859895-T-C

173933464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31860051-G-A

173933588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31860247-T-A

173933738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31860407-G-C

173934846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31861579-A-G

173935156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31861823-A-G

http://identifiers.org/hco/5/GRCh38#173936316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31864501-A-C

173936316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31864501-A-G

173936333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31864517-C-T

173936431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31864608-C-T

http://identifiers.org/hco/5/GRCh38#173936814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31864953-C-A

173936814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31864953-C-G

173936814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31864953-C-T

173937932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31865341-A-G

173938102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31865458-A-T

http://identifiers.org/hco/5/GRCh38#173939480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31865644-A-C

http://identifiers.org/hco/5/GRCh38#173939781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31865916-C-A

173939781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31865916-C-G

173940292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866131-C-T

173940657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866405-C-G

173940775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866508-T-C

173940775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866508-T-G

173940932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866657-G-C

http://identifiers.org/hco/5/GRCh38#173941012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31866718-A-C

173941037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866753-A-G

173941061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866777-A-G

173941244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866948-C-T

173941274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31866979-A-G

173941326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31867023-C-T

173941328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31867025-T-G

173941420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31867123-A-G

173942335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31868133-A-G

173942447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31868231-G-A

173942772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31868556-C-T

http://identifiers.org/hco/5/GRCh38#173942892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31868671-C-A

173942892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31868671-C-T

173943163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31868936-T-C

173943485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31869209-A-G

173943582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31869284-A-T

http://identifiers.org/hco/5/GRCh38#173944013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31869697-A-C

173944283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31869942-G-A

173944613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31870085-A-G

173944613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31870085-A-T

173944731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31870198-T-A

173944826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31870283-T-C

173944968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 31870410-T-G

173945167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31870617-G-A

http://identifiers.org/hco/5/GRCh38#173945200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31870646-C-A

173945200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31870646-C-G

http://identifiers.org/hco/5/GRCh38#173945227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31870680-C-A

173945227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31870680-C-T

173945248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31870703-G-A

http://identifiers.org/hco/5/GRCh38#173945249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31870704-C-A

173945249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31870704-C-T

173945488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31870923-C-T

173946020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31871384-G-C

173946343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31871624-G-A

173946621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31871824-A-G

173946625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31871828-G-T

173946812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31872009-C-T

173946861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31872059-A-G

173947568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31872109-C-T

173947750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31872287-G-A

173947768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31872306-T-C

173949102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31873904-A-G

173949584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31874702-T-C

173949609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31874727-G-T

173949621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31874738-T-A

173949621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31874738-T-C

http://identifiers.org/hco/5/GRCh38#173949678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31874797-C-A

173949678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31874797-C-T

http://identifiers.org/hco/5/GRCh38#173949715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31874834-C-A

173951330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31877252-C-T

173951702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31877545-G-C

173951812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31877631-T-C

173951998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31877812-A-G

173951998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31877812-A-T

173952044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31877862-G-A

173952044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31877862-G-C

173952044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31877862-G-T

173952046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31877864-T-A

173952046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31877864-T-C

173952386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31878162-T-A

173952425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31878191-G-A

173952528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31878276-G-A

173952733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31879700-T-A

173952733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31879700-T-C

173952744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31879720-T-C

173952956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31879908-T-G

173953030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31879983-G-A

173953057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31880010-T-C

173953059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31880012-T-C

173953075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31880024-T-G

173953161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: missense variant
orthologous variants: 31880108-G-T

173955481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881010-A-T

173955780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881191-T-A

173955780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881191-T-C

173955782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881193-A-T

http://identifiers.org/hco/5/GRCh38#173955783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31881194-A-C

173955783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881194-A-G

173955813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881221-G-A

173955813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881221-G-T

173955838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881233-G-A

173955838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: intron variant
orthologous variants: 31881233-G-T

173956186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31881585-C-G

173956186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31881585-C-T

http://identifiers.org/hco/5/GRCh38#173956400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31881799-C-A

173956553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31881936-G-A

173956553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31881936-G-T

173956632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31881998-C-T

173957354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31882681-A-G

173957915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31883234-A-G

173958768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31884097-A-T

http://identifiers.org/hco/5/GRCh38#173959297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31884625-C-A

173959297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31884625-C-T

173960414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31885733-A-G

http://identifiers.org/hco/5/GRCh38#173960422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#31885741-C-A

173960422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31885741-C-G

173960442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31885761-G-T

173960477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31885797-G-A

173960477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31885797-G-T

173960502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31885821-G-A

173960502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31885821-G-T

173960911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31886099-G-A

173960985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31886165-G-T

173961075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31886250-G-A

173961075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31886250-G-T

173961120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31886299-G-T

173961163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21747
most severe consequence: 3 prime UTR variant
orthologous variants: 31886378-A-G