186104445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5 prime UTR variant
orthologous variants: 45835541-A-G

186104480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5 prime UTR variant
orthologous variants: 45835507-G-T

http://identifiers.org/hco/4/GRCh38#186104494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45835491-C-A

186104501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45835484-G-A

186104501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45835484-G-T

186104516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45835469-G-A

186104516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45835469-G-T

186104606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, undefined
orthologous variants: 45835366-G-A

186104606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, undefined
orthologous variants: 45835366-G-T

186104787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45835176-C-G

186104790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45835173-C-G

186104859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45835087-T-A

186104859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45835087-T-C

186104859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45835087-T-G

http://identifiers.org/hco/4/GRCh38#186104928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45835001-C-A

186104928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45835001-C-T

186105004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834907-G-A

186105004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834907-G-T

186105038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834834-C-G

186105038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834834-C-T

186105046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834826-G-A

186105046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834826-G-T

186105056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834816-C-G

186105056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834816-C-T

186105174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834704-G-A

186105174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834704-G-C

186105174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834704-G-T

186105176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834702-G-A

186105176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834702-G-T

http://identifiers.org/hco/4/GRCh38#186105199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45834679-C-A

186105199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45834679-C-G

186105199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45834679-C-T

http://identifiers.org/hco/4/GRCh38#186105377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45834489-C-A

http://identifiers.org/hco/4/GRCh38#186105394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45834472-C-A

186105394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45834472-C-G

186105394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45834472-C-T

http://identifiers.org/hco/4/GRCh38#186105396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45834470-C-A

186105396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834470-C-T

186105416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834444-T-A

186105416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834444-T-C

186105416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant
orthologous variants: 45834444-T-G

http://identifiers.org/hco/4/GRCh38#186105468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#45834368-C-A

186105468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834368-C-G

186105468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834368-C-T

186105483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834353-T-A

186105483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834353-T-C

186105483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834353-T-G

186105495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834341-T-C

http://identifiers.org/hco/4/GRCh38#186105554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45834279-C-A

186105554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834279-C-T

186105611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834222-G-A

186105611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834222-G-T

186105620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834213-G-A

186105620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834213-G-C

186105620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834213-G-T

186105626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834207-T-C

186105626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45834207-T-G

186105689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45834155-C-G

186105860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45834051-C-G

186105870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45834030-C-T

186105972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833920-C-T

186105989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833903-A-G

186106019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45833874-A-T

186106226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833696-C-G

186106226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833696-C-T

186106354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833517-A-G

186107089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833263-G-T

186107261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833091-G-A

186107261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833091-G-T

186107741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832938-T-C

186107757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832917-A-G

186107781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832893-A-G

http://identifiers.org/hco/4/GRCh38#186107786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45832888-C-A

186107815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832859-G-A

186107815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832859-G-T

186107827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832847-G-T

http://identifiers.org/hco/4/GRCh38#186107836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45832838-A-C

186107836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832838-A-G

186107837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832835-G-T

186107848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832824-G-T

186107860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832815-G-T

186107922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832761-C-T

186108240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832498-A-G

186108275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832467-C-T

186108653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832093-G-T

186109997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831820-G-A

186109997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831820-G-C

http://identifiers.org/hco/4/GRCh38#186110050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45831760-C-A

186110052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831758-C-T

186110170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831653-G-A

186110197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831626-A-G

186110229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831596-A-G

186110277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831550-T-A

186110285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831542-T-A

186110285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831542-T-C

186110295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831532-G-C

http://identifiers.org/hco/4/GRCh38#186110353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45831463-A-C

186110353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831463-A-G

186110364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831451-G-A

186116437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831420-A-G

186116838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830657-A-G

http://identifiers.org/hco/4/GRCh38#186116873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45830625-C-A

186116894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830602-G-A

http://identifiers.org/hco/4/GRCh38#186116900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45830596-C-A

186116900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830596-C-G

186116900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830596-C-T

http://identifiers.org/hco/4/GRCh38#186116916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45830580-C-A

186116972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830534-A-T

186117026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830481-C-T

186117268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830149-G-A

http://identifiers.org/hco/4/GRCh38#186117325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45830086-C-A

http://identifiers.org/hco/4/GRCh38#186117386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45830039-C-A

186119289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45829944-G-A

186119425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45829837-A-G

186119521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45829746-T-C

186119643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45829589-T-C

186119980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45828874-G-A

186120032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45828818-A-G

186120088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45828759-G-T

186120184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45828680-C-T

http://identifiers.org/hco/4/GRCh38#186120299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45828567-C-A

186121192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45828002-G-A

186121196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827998-T-C

186121261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827930-C-T

186121347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827848-G-A

186121350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827845-C-G

186121358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827837-C-T

186121367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827832-C-G

186121485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827725-T-C

186121506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827704-G-A

186121644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827587-G-A

186121644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827587-G-T

186121681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827557-C-T

http://identifiers.org/hco/4/GRCh38#186121693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45827554-C-A

186121693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827554-C-G

186121941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827314-G-T

186121958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827297-T-A

186121959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827296-C-G

http://identifiers.org/hco/4/GRCh38#186121987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45827285-A-C

186122098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827164-A-G

186122128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45827125-T-C

186125457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826890-G-A

186125464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826883-G-A

http://identifiers.org/hco/4/GRCh38#186125496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45826859-C-A

186125496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826859-C-T

186125543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826828-G-C

http://identifiers.org/hco/4/GRCh38#186125555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45826816-C-A

186125556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826815-A-G

186125604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826776-T-C

186125614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826761-A-T

186125621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826754-T-C

186125621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826754-T-G

186125686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826692-C-T

186125695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826682-T-C

186125729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826648-G-C

http://identifiers.org/hco/4/GRCh38#186125730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45826647-C-A

186125730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45826647-C-T

186128295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45825862-C-G

186128478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45825660-A-G

186128607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45825531-T-C

186128621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45825514-G-C

186128651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45825483-T-C

186128706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45825446-T-C

186129281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45825327-G-T

http://identifiers.org/hco/4/GRCh38#186129294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45825314-C-A

186129395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45825250-C-T

186129540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45825142-C-T

186129852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824840-A-T

186129858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824834-G-A

http://identifiers.org/hco/4/GRCh38#186129921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45824769-C-A

186129921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824769-C-T

http://identifiers.org/hco/4/GRCh38#186129997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45824693-C-A

186129997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824693-C-T

186130001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824690-G-A

186130001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824690-G-T

186130021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45824670-A-T

186130029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45824663-A-G

186130117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45824592-C-T

186130139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45824571-A-G

186130145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45824565-A-T

186130149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45824561-T-G

186130162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824548-G-A

http://identifiers.org/hco/4/GRCh38#186130322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45824435-A-C

186130322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824435-A-G

http://identifiers.org/hco/4/GRCh38#186130327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45824430-C-A

186130327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824430-C-T

186130372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824393-A-G

http://identifiers.org/hco/4/GRCh38#186131842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45821886-C-A

186131842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45821886-C-T

http://identifiers.org/hco/4/GRCh38#186135498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45818554-C-A

186135598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45818456-C-T

186135660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45818388-A-G

186135665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45818383-C-G

186135665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45818383-C-T

186135678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45818369-C-T

http://identifiers.org/hco/4/GRCh38#186135679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45818368-A-C

186135793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45818255-T-C

186136652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45817506-T-A

186136692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45817473-A-G

186137339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815866-T-C

186137349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815859-T-C

186137352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815856-G-C

186137451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815781-G-A

186137461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45815771-C-T

186137493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815739-A-T

186137535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815697-C-T

186141579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814925-A-T

186141643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814771-G-C

186141717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814691-A-G

186141719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814689-C-T

186141723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814685-G-C

186141832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814568-C-T

186141929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814472-C-T

186141996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814407-C-T

186142225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814239-G-A

186142225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814239-G-T

186142255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814208-T-C

186144391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45812181-G-A

186144423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45812161-G-T

186144659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45811931-G-A

186144659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45811931-G-T

186144689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45811902-G-A

186144689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45811902-G-T

http://identifiers.org/hco/4/GRCh38#186144703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45811891-C-A

186144703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45811891-C-T

186144752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811862-G-C

186144752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811862-G-T

http://identifiers.org/hco/4/GRCh38#186144780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45811819-A-C

186144780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811819-A-G

http://identifiers.org/hco/4/GRCh38#186144782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45811817-C-A

186144782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811817-C-T

186144807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811794-G-A

186144807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811794-G-T

http://identifiers.org/hco/4/GRCh38#186144825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45811770-C-A

186144825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811770-C-T

186144894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45811674-C-T

186144902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45811649-G-T

186144918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811633-C-T

186144920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811631-G-A

186145097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45811448-G-T

http://identifiers.org/hco/4/GRCh38#186145129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45811409-A-C

186145129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811409-A-G

186145178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811360-C-G

http://identifiers.org/hco/4/GRCh38#186145185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45811347-C-A

186145185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811347-C-G

186145185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811347-C-T

186145197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811335-G-A

186145197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811335-G-T

186145207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811325-G-A

186145207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811325-G-C

186145207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45811325-G-T

186145265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811240-G-A

186145321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811156-T-A

186145337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811139-C-T

186145365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811097-G-A

186145730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810656-T-C

186147728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810046-T-G

186148702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809172-T-C

186148752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809117-T-C

186149087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808830-G-A

186149158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808779-T-C

186149320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808621-A-G

186149463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808498-A-T

186149475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808486-A-G

186149590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 45808381-C-T

186149600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45808371-C-T

186149606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45808365-C-G

186149606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45808365-C-T

http://identifiers.org/hco/4/GRCh38#186149617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45808354-C-A

186149617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45808354-C-T

186149639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45808332-G-A

186149642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45808329-A-T

186149657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45808314-A-G

186149660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45808311-G-A

186149743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808228-G-A

186149743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808228-G-T

http://identifiers.org/hco/4/GRCh38#186149756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45808218-A-C

186149756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808218-A-G

186151614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807322-A-G

186151703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807236-C-G

186151703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807236-C-T

186151726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807213-T-G

186151793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807148-G-A

186151793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807148-G-T

186151798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807143-A-G

186151817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807128-G-T

186151931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45806968-T-C

186152059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806852-G-A

http://identifiers.org/hco/4/GRCh38#186152094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45806815-C-A

186152094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806815-C-T

186152121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806788-G-A

186152121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806788-G-C

186152381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806556-A-G

186152416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806465-G-A

186152416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806465-G-C

http://identifiers.org/hco/4/GRCh38#186152444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45806427-C-A

186152513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806364-G-A

186152513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806364-G-T

186152938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806283-G-A

186152987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806234-T-G

186153097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805943-T-A

186153170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805868-G-A

186153170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805868-G-C

186153186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805854-A-G

186153199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805836-A-G

186153219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805819-G-A

186153219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805819-G-C

http://identifiers.org/hco/4/GRCh38#186153237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45805801-C-A

186153237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805801-C-T

http://identifiers.org/hco/4/GRCh38#186153338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45805135-A-C

186153463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45805000-G-A

http://identifiers.org/hco/4/GRCh38#186153533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45804943-C-A

186153533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804943-C-G

186153533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804943-C-T

http://identifiers.org/hco/4/GRCh38#186153535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45804941-C-A

186153535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804941-C-T

http://identifiers.org/hco/4/GRCh38#186153553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45804924-C-A

186153553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804924-C-G

186153553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804924-C-T

186153564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804913-A-G

186153591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804883-A-G

186153592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804882-C-T

186153628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804843-T-C

186153757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45804711-A-G

http://identifiers.org/hco/4/GRCh38#186153783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45804610-A-C

186153792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804601-T-C

186153792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804601-T-G

186153813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804518-A-G

186153818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804513-A-G

186153846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804486-T-C

186153891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804437-A-G

186153983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804346-A-T

186154016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804313-T-C

186154045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804286-T-A

186154200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804121-C-T

186154211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804109-G-T

186154275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804055-C-T

186154289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804041-A-G

186154371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803699-T-C

http://identifiers.org/hco/4/GRCh38#186154394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45803676-C-A

186154394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803676-C-T

186154405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803665-G-A

186154405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803665-G-C

186154405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803665-G-T

186154455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803616-T-A

186154455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803616-T-C

http://identifiers.org/hco/4/GRCh38#186154538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45803536-A-C

186154538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45803536-A-G

186154544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45803530-G-A

186154544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45803530-G-C

186154544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45803530-G-T

186154558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45803516-G-A

186154562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45803512-C-T

186154591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45803483-T-C

186154677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803399-A-T

186154805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803295-G-A

186154814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803286-G-A

186154851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803212-A-G

186154851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803212-A-T

186154888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803176-G-C

186154905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803159-C-G

186154963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45803103-T-A

186155908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45802382-G-A

186155918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45802299-A-T

186155928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45802289-A-G

186155930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45802285-G-C

186155930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45802285-G-T

186156029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45802147-C-T

186156052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45802124-A-G

186156052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45802124-A-T

186156154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45802022-G-A

186156154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45802022-G-C

186156154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45802022-G-T

186156185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45801991-T-G

http://identifiers.org/hco/4/GRCh38#186156206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45801970-A-C

http://identifiers.org/hco/4/GRCh38#186156260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45801916-C-A

186156274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801895-A-G

186156274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801895-A-T

186157351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801792-C-T

186157353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801790-A-G

186157422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801723-G-A

186157422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801723-G-T

186157430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801710-T-A

186157430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801710-T-G

186157441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801699-G-A

186157441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801699-G-T

186157600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45801596-G-A

186157623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45801573-C-T

186157639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45801557-G-A

http://identifiers.org/hco/4/GRCh38#186157656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45801540-C-A

186157656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45801540-C-T

186157675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45801521-G-A

186157675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45801521-G-C

http://identifiers.org/hco/4/GRCh38#186157733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45801463-C-A

186157733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801463-C-T

186157762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801428-G-A

186157762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801428-G-C

186157762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801428-G-T

http://identifiers.org/hco/4/GRCh38#186159937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45800046-C-A

http://identifiers.org/hco/4/GRCh38#186162842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45798113-C-A

186162842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45798113-C-T

http://identifiers.org/hco/4/GRCh38#186162845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45798110-A-C

186162845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 45798110-A-G

186162845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 45798110-A-T

186162953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45798002-G-A

186163131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797929-A-G

186163202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797859-C-T

186163394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797728-G-A

186163455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45797665-G-A

186163646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797479-T-C

186163656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797469-T-C

186163656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797469-T-G

186163662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797463-A-G

http://identifiers.org/hco/4/GRCh38#186163677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45797449-C-A

186163707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797419-T-C

186163852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797277-G-A

186163855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797274-A-G

186163871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797258-G-A

186163919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797209-T-G

186163943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45797190-A-G

186165413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45795477-C-G

186165413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45795477-C-T

http://identifiers.org/hco/4/GRCh38#186165421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45795469-C-A

186165421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45795469-C-G

186165421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45795469-C-T

186165444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45795446-C-T

186165447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45795443-G-A

186165597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45795300-A-G

186165597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45795300-A-T

186165630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45795271-A-G

186165783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45795136-C-T

186166053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794895-G-C

186166063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794885-G-A

186166067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794881-A-G

186166085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794862-G-A

186166085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794862-G-C

186166085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794862-G-T

http://identifiers.org/hco/4/GRCh38#186166182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45794776-A-C

186166686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794611-T-A

186166741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794558-A-G

186166741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794558-A-T

http://identifiers.org/hco/4/GRCh38#186166860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45794444-C-A

186167001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45794286-A-G

186167062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45794225-G-A

186167079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45794208-A-G

186167113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794174-C-T

186167214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45794066-C-G

186167214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45794066-C-T

186167353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793737-G-A

186167353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793737-G-T

186167389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45793697-G-T

http://identifiers.org/hco/4/GRCh38#186167393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45793693-C-A

186167393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45793693-C-T

http://identifiers.org/hco/4/GRCh38#186167400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45793682-C-A

186167400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45793682-C-G

186167400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45793682-C-T

186167406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793676-T-G

http://identifiers.org/hco/4/GRCh38#186167407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45793675-C-A

186167407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793675-C-T

186167426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793664-G-A

186167426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793664-G-C

186167426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793664-G-T

186167457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793640-G-T

http://identifiers.org/hco/4/GRCh38#186167462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45793635-C-A

186167462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793635-C-T

186167470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793629-G-T

http://identifiers.org/hco/4/GRCh38#186167488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45793611-C-A

186167488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793611-C-T

186167500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793600-G-T

http://identifiers.org/hco/4/GRCh38#186167507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45793593-C-A

186167507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45793593-C-T

186167538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45793558-T-A

186167631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45793469-T-A

http://identifiers.org/hco/4/GRCh38#186167636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45793465-A-C

186167716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45793408-T-A

186167716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45793408-T-C

186167729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45793395-G-T

186167753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45793368-G-T

186171454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792840-C-T

186171455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792839-G-A

186171455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792839-G-C

186171471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792823-A-T

186171512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792784-T-A

186171814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792509-T-C

186171847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792474-A-G

186171864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792455-G-A

186171864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792455-G-C

186171864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792455-G-T

186171866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792453-G-A

http://identifiers.org/hco/4/GRCh38#186171876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45792444-C-A

186171876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792444-C-T

186171880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: intron variant
orthologous variants: 45792440-T-G

http://identifiers.org/hco/4/GRCh38#186171964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45792357-A-C

186171964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: missense variant
orthologous variants: 45792357-A-T

186172004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 45792317-C-T

http://identifiers.org/hco/4/GRCh38#186172005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45792316-C-A

186172005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 45792316-C-T

186172033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 45792279-T-A

186172033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 45792279-T-G

186172039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 45792273-T-A

186172080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792225-T-C

186172124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792177-T-C

186172191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792110-G-A

186172191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792110-G-T

http://identifiers.org/hco/4/GRCh38#186172192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45792109-C-A

186172192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792109-C-T

http://identifiers.org/hco/4/GRCh38#186172235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45792059-C-A

186172235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792059-C-G

186172251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792043-G-T

186172255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792039-G-A

186172255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45792039-G-T

http://identifiers.org/hco/4/GRCh38#186172326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45792001-A-C

186172365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45791963-G-A

http://identifiers.org/hco/4/GRCh38#186172468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45791866-C-A

186172527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45791747-T-G

186172534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45791742-G-T

186172541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45791723-C-T

186172797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45791477-T-C

186173343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45791009-C-T

186173685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45790988-C-T

186173719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45790956-G-A

186174574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45790474-A-G

186174723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45790328-G-A

186174727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45790324-T-G

186175314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24527
most severe consequence: 3 prime UTR variant
orthologous variants: 45789728-A-G