154391633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056716-T-C

154391689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056770-C-T

154391729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056807-G-C

154391747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056825-G-T

154391783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056864-A-T

154391786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056867-T-C

154391818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056893-G-A

154391818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056893-G-C

154391818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7056893-G-T

154392364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057323-G-A

154392396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057350-G-T

154392408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057366-G-T

154392493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057418-A-G

154392493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057418-A-T

154392709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057515-G-T

154392820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057629-A-G

154392830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7057639-G-C

154393732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7060728-C-G

154393787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7060788-T-C

154394404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061098-C-T

154394467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061150-T-C

154394510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061189-G-T

154394583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061285-G-T

154394593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061296-G-A

154394693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061431-T-C

http://identifiers.org/hco/6/GRCh38#154394821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7061542-C-A

154394821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061542-C-G

http://identifiers.org/hco/6/GRCh38#154394825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7061546-C-A

154394855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061574-G-A

154394874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061593-G-A

154395113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061846-G-A

154395113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7061846-G-T

154395467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062181-T-C

154395715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062406-A-G

154395721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062412-C-G

154395721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062412-C-T

154395731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062422-A-G

154395739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062430-A-G

154397232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062828-G-T

154397235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062831-A-G

154397308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7062908-C-T

154397552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7063085-G-C

154397615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7063146-G-A

154399346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 7064107-A-G

154399347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 7064108-A-G

http://identifiers.org/hco/6/GRCh38#154399423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7064163-C-A

154399460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064200-G-T

154399474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064214-G-T

http://identifiers.org/hco/6/GRCh38#154399492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7064230-C-A

154399651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064384-T-C

154399653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064386-C-G

154399653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064386-C-T

154399666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064399-A-G

154399962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064634-T-C

154399968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064640-A-G

http://identifiers.org/hco/6/GRCh38#154399997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7064672-C-A

http://identifiers.org/hco/6/GRCh38#154400141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7064866-C-A

http://identifiers.org/hco/6/GRCh38#154400221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7064909-C-A

http://identifiers.org/hco/6/GRCh38#154400222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7064910-C-A

154400248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7064935-A-G

http://identifiers.org/hco/6/GRCh38#154400342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7065024-C-A

154400342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065024-C-T

http://identifiers.org/hco/6/GRCh38#154400406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7065088-C-A

http://identifiers.org/hco/6/GRCh38#154400407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7065089-C-A

154400407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065089-C-T

154400411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065092-G-C

154400664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065338-T-C

http://identifiers.org/hco/6/GRCh38#154400678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7065352-C-A

154400678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065352-C-T

154400802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065472-A-G

154400850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065515-T-C

http://identifiers.org/hco/6/GRCh38#154400886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7065536-C-A

154400893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065543-G-A

154400927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065567-G-A

154400927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065567-G-T

154401074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065686-T-C

154401206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7065878-T-C

154401635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7066272-C-G

154401752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7066379-T-C

154401817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7066446-G-T

154401841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7066471-G-A

154401876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7066505-G-A

http://identifiers.org/hco/6/GRCh38#154403565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7068149-C-A

154403624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068210-T-C

http://identifiers.org/hco/6/GRCh38#154403678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7068270-C-A

154404027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068604-G-A

154404027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068604-G-C

154404053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068630-T-C

154404919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068843-C-T

154404969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068901-T-A

154404969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068901-T-C

154404997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068924-C-G

154405017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7068943-G-T

154405101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3 prime UTR variant
orthologous variants: 7069016-A-G

154405534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069460-A-G

154405791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069718-G-T

154405792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069719-T-C

http://identifiers.org/hco/6/GRCh38#154405805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7069735-C-A

http://identifiers.org/hco/6/GRCh38#154405820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7069754-C-A

154405821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069755-T-C

154405853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069778-T-A

154405853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069778-T-G

154405854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069779-G-A

154405885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069811-G-A

154405927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069852-G-A

154405931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069856-T-G

http://identifiers.org/hco/6/GRCh38#154405960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7069885-C-A

154405961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069886-A-G

154405974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069907-G-T

154405992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069925-G-T

154406008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069946-T-C

http://identifiers.org/hco/6/GRCh38#154406026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7069964-A-C

154406051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069983-G-A

154406051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7069983-G-T

154406077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070009-G-T

154406080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070012-C-G

154406080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070012-C-T

http://identifiers.org/hco/6/GRCh38#154406094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7070026-C-A

154406107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070039-A-G

http://identifiers.org/hco/6/GRCh38#154406109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7070041-C-A

154406109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070041-C-T

154406131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070067-T-C

154406187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070122-T-C

http://identifiers.org/hco/6/GRCh38#154406188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7070123-C-A

http://identifiers.org/hco/6/GRCh38#154406255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7070189-C-A

154406255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7070189-C-T

154406540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7070474-G-A

154408545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7074819-C-G

154408596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7074859-G-A

154408671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7074931-T-C

http://identifiers.org/hco/6/GRCh38#154408776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7075021-A-C

154408803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7075054-T-A

154409066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7075260-G-A

154409211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7075379-T-C

154409411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7075721-T-G

154409542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7075819-C-G

http://identifiers.org/hco/6/GRCh38#154410205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7075963-C-A

154410321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076073-G-C

154410321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076073-G-T

154410404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7076156-A-T

http://identifiers.org/hco/6/GRCh38#154410561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7076312-A-C

154410648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076382-T-C

154410759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076462-G-A

154410795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076498-T-C

http://identifiers.org/hco/6/GRCh38#154410921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7076621-A-C

154410935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 7076636-A-G

154410973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7076674-T-C

154411013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7076714-T-A

154411013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7076714-T-C

154411076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7076777-C-T

154411136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7076837-C-G

http://identifiers.org/hco/6/GRCh38#154411222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7076925-C-A

154411222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076925-C-T

http://identifiers.org/hco/6/GRCh38#154411223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7076926-C-A

154411223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076926-C-T

http://identifiers.org/hco/6/GRCh38#154411226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7076929-C-A

154411308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7076989-T-C

http://identifiers.org/hco/6/GRCh38#154411795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7077184-C-A

154411997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7077341-A-G

154412294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7077619-C-G

154412611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7077910-C-G

154412611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7077910-C-T

http://identifiers.org/hco/6/GRCh38#154412672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7077981-A-C

154412795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078080-T-G

154413039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078308-C-T

154413057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078327-C-T

http://identifiers.org/hco/6/GRCh38#154413068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7078337-C-A

http://identifiers.org/hco/6/GRCh38#154413583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7078731-A-C

http://identifiers.org/hco/6/GRCh38#154413604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7078752-C-A

154413668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7078816-T-A

http://identifiers.org/hco/6/GRCh38#154414288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7079012-C-A

154414288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079012-C-T

154414292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7079016-A-G

154414331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7079055-A-T

154414412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 7079136-T-C

154414465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079191-A-G

154414465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079191-A-T

154414483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079209-G-A

http://identifiers.org/hco/6/GRCh38#154414493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7079214-C-A

154414493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7079214-C-T

154414522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7079241-G-C

154414522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7079241-G-T

154414603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079317-T-C

154414630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079325-A-G

154414631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079326-T-C

154414631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079326-T-G

154414648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079331-G-A

154414648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079331-G-T

154414714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079393-T-A

154414714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7079393-T-C

154415815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080096-A-G

http://identifiers.org/hco/6/GRCh38#154415934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7080199-A-C

154415958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080223-T-C

154415981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080246-A-T

154416587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080572-G-A

http://identifiers.org/hco/6/GRCh38#154416784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7080757-A-C

154416966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080906-C-G

154416966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080906-C-T

154417442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081288-G-T

154417573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081404-C-G

154417708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081514-A-G

154417835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081623-C-T

154417926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7081723-T-C

http://identifiers.org/hco/6/GRCh38#154417943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7081740-C-A

154418413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082111-T-A

154418413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082111-T-C

154422297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084324-T-C

http://identifiers.org/hco/6/GRCh38#154422366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7084389-C-A

154422366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084389-C-T

154422379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084402-G-A

154422379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084402-G-C

154422379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084402-G-T

154422406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084434-G-C

154422406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084434-G-T

154422569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7084585-G-A

154422715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084707-T-C

http://identifiers.org/hco/6/GRCh38#154423003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7085136-C-A

154423003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085136-C-G

154423003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085136-C-T

154423181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085289-T-A

154423235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085341-C-T

154423554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085349-A-G

154423607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085402-A-G

154423613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085427-T-C

154424309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085969-T-C

154424458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086097-A-G

154424458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086097-A-T

154424564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086200-A-G

154425971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086729-C-G

154425976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086734-T-G

154426066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086806-T-C

154426172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086919-A-G

154426711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087241-G-A

http://identifiers.org/hco/6/GRCh38#154427905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7088093-C-A

154427906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088094-T-A

154427956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088144-T-A

154427956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088144-T-C

154428007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088226-G-C

154428007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088226-G-T

154428053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088284-T-C

154428089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088317-A-T

154428107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088334-A-G

154428164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7088391-A-G

154428164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 7088391-A-T

154428208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088435-A-G

154428222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088447-C-T

154428247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088469-G-A

154428247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088469-G-T

http://identifiers.org/hco/6/GRCh38#154428299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7088504-A-C

154428299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088504-A-G

154428314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088520-G-A

154428314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088520-G-C

154428314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088520-G-T

154428456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088628-T-C

http://identifiers.org/hco/6/GRCh38#154428988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7089035-C-A

154428988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089035-C-G

154429159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089174-A-G

154429183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089207-G-C

154429410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089356-C-G

154429466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089412-G-C

154429776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089689-T-C

154429996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089858-C-G

154429996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089858-C-T

154430177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090039-A-G

154430348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090202-G-A

154430348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090202-G-T

154430364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090222-A-G

154430364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090222-A-T

154430367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090225-T-A

http://identifiers.org/hco/6/GRCh38#154430371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7090229-C-A

http://identifiers.org/hco/6/GRCh38#154430393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7090251-C-A

154430393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090251-C-T

154430399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090257-G-A

http://identifiers.org/hco/6/GRCh38#154430677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7090508-C-A

154430677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090508-C-G

154430739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7090570-T-A

http://identifiers.org/hco/6/GRCh38#154430910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7090719-C-A

154431005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7090807-C-T

154431616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091061-T-C

154431640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091086-T-C

154431828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091275-G-A

154431835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091282-T-A

154431915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091360-A-G

154432137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091583-G-A

154432137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091583-G-T

154432171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091614-T-A

154432225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7091654-T-C

154432527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092027-T-C

154432881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092359-G-A

154432901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7092379-T-G

154432957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092436-G-A

154432993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092471-A-G

154433043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092520-T-C

154433078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092555-C-T

154433156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092633-C-T

154433375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092871-T-C

154433443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092938-T-C

154433650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093924-G-A

154433650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093924-G-C

154433650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093924-G-T

154433671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093945-T-C

154433671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093945-T-G

154433684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093958-G-T

154433748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094019-A-G

154433752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094023-G-A

154433752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094023-G-T

154433874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7094242-G-T

http://identifiers.org/hco/6/GRCh38#154433881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7094249-C-A

154433881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7094249-C-T

154433884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7094252-G-A

154433884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7094252-G-C

154433884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7094252-G-T

154433898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7094266-G-A

154434265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7094664-C-T

154434307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7094705-G-T

154434321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7094719-G-A

154434491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095113-A-G

http://identifiers.org/hco/6/GRCh38#154434505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7095127-C-A

154434919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095526-A-G

154434936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095540-G-A

http://identifiers.org/hco/6/GRCh38#154435469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7095726-C-A

154435469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095726-C-G

154435504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095744-C-T

154435517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095757-G-A

154435517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095757-G-C

154435536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095770-T-C

154435536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7095770-T-G

154436908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7096494-A-G

154436908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7096494-A-T

154436937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7096523-G-A

154437970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097534-G-A

154437993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097552-C-T

154438042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097606-C-T

http://identifiers.org/hco/6/GRCh38#154438044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7097608-C-A

154438164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097756-T-A

154438164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097756-T-C

154438187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097776-T-C

154438270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097925-T-C

154438272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097927-T-A

154438339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7097997-G-A

154438364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7098046-C-T

154438560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7098414-T-G

154438580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7098434-G-A

154438591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7098444-C-G

154438869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7098536-A-G

http://identifiers.org/hco/6/GRCh38#154438892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7098558-A-C

http://identifiers.org/hco/6/GRCh38#154438933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7098582-C-A

154439020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7098674-T-A

154439025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7098680-C-T

154439282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7099818-T-C

154439410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7099971-C-T

http://identifiers.org/hco/6/GRCh38#154439415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7099976-C-A

154439415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7099976-C-G

154439415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7099976-C-T

154439442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7100083-C-T

154439553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7100175-A-G

154440056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7100387-T-C

154440075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7100406-C-T

154440076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7100407-A-G

154440156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, undefined
orthologous variants: 7100469-G-A

http://identifiers.org/hco/6/GRCh38#154440212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7100527-A-C

http://identifiers.org/hco/6/GRCh38#154440330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7100638-C-A

154440477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102238-T-C

154440547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102296-C-T

154440657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102382-T-C

154440732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102447-A-T

154440763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102465-G-A

154440909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102578-G-T

154440945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102611-C-G

154440958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102623-A-G

http://identifiers.org/hco/6/GRCh38#154440987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7102659-C-A

154440987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102659-C-T

154441189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102769-G-A

154441189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102769-G-C

154441261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102832-A-G

http://identifiers.org/hco/6/GRCh38#154441267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7102838-A-C

154441267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102838-A-G

154441267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102838-A-T

154441278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102850-G-A

154441278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102850-G-C

154441278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102850-G-T

154441288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102860-T-A

154441288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102860-T-C

154441289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102861-G-A

154441289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102861-G-C

154441289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102861-G-T

154441367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: synonymous variant
orthologous variants: 7102939-T-C

http://identifiers.org/hco/6/GRCh38#154441394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7102966-C-A

154441394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102966-C-G

154441415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102992-G-C

154441415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7102992-G-T

http://identifiers.org/hco/6/GRCh38#154441827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7103828-A-C

http://identifiers.org/hco/6/GRCh38#154441939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7104143-A-C

154441949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7104153-T-A

154441949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7104153-T-C

154441981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7104185-G-T

154442046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7104250-A-G

154442078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7104273-T-G

http://identifiers.org/hco/6/GRCh38#154442153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7104348-A-C

154442254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: missense variant
orthologous variants: 7104449-C-T

http://identifiers.org/hco/6/GRCh38#154442261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7104456-C-A

http://identifiers.org/hco/6/GRCh38#154442307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7104503-C-A

154442320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7104516-T-G

154445537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107063-A-G

154446336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107147-C-T

154446337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107148-G-A

154446408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107209-T-G

154446417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107218-T-C

154446456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107250-T-A

154446477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107271-C-T

154446484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107277-C-T

154446554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107349-T-C

154447263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107643-G-A

154447274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107654-G-A

154447364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7107740-T-C

154447816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7108081-C-T

154447972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7108238-A-T

http://identifiers.org/hco/6/GRCh38#154448396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7108688-C-A

154448456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7108737-T-A

154448456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7108737-T-C

154448532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7108814-G-C

154448793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7109075-A-G

http://identifiers.org/hco/6/GRCh38#154449073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7109360-C-A

http://identifiers.org/hco/6/GRCh38#154450066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7110619-C-A

154450066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110619-C-G

154450066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110619-C-T

http://identifiers.org/hco/6/GRCh38#154450291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7110842-C-A

154450291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110842-C-T

http://identifiers.org/hco/6/GRCh38#154450311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7110856-C-A

154450311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110856-C-T

154450331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110876-G-A

154450331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110876-G-T

154450383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110904-T-C

154450405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110919-G-A

154450405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110919-G-T

154450432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7110931-G-C

154450538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111034-C-T

154450579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111076-G-A

154450688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111171-G-A

154450688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111171-G-T

154450732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111204-T-A

154450777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111249-T-C

154451974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111528-G-A

http://identifiers.org/hco/6/GRCh38#154452264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7111866-C-A

http://identifiers.org/hco/6/GRCh38#154452330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7111932-C-A

154452363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111965-G-A

http://identifiers.org/hco/6/GRCh38#154452394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7111993-A-C

154452394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7111993-A-G

154452488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7112063-A-G

154452663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7112239-T-C

154452663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7112239-T-G

http://identifiers.org/hco/6/GRCh38#154452679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7112267-A-C

154452766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7112331-A-G

154453107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7112625-A-T

154453370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113003-T-C

154453414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113046-G-C

http://identifiers.org/hco/6/GRCh38#154453461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7113077-A-C

154453502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113115-G-A

154453514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113127-T-A

154453551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113151-A-G

154453592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113192-A-T

154453732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113333-G-A

154453732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113333-G-C

154453732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113333-G-T

154453914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113484-G-T

http://identifiers.org/hco/6/GRCh38#154453998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7113553-A-C

http://identifiers.org/hco/6/GRCh38#154454147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7113577-A-C

154454147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113577-A-G

154454170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113600-T-A

154454170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113600-T-C

154454170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113600-T-G

154454368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7113757-G-T

154457746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116312-C-T

154457949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116492-C-G

154458061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116599-T-C

154458121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116628-T-C

154458123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116630-G-C

154458215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116678-G-C

154458446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116842-C-T

154458626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7116970-C-T

154458828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7117140-G-C

http://identifiers.org/hco/6/GRCh38#154458852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7117164-A-C

154458869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7117181-G-A

154458869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7117181-G-C

154459032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7117336-T-A

154459032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7117336-T-G

http://identifiers.org/hco/6/GRCh38#154459705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7117888-A-C

154463997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7121545-G-A

154464119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7121618-T-C

154465000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122163-G-C

154465123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122274-T-A

154465123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122274-T-G

154465143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122294-A-T

154465265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122373-T-C

154465339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122447-T-C

154465373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122475-G-A

154465378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122480-A-G

154465386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122488-A-G

154465563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122650-C-T

154465625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122711-G-A

154465625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122711-G-T

154465708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7122792-G-C

154466162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7123208-G-A

154466237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7123278-T-C

154466238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7123279-A-T

154466349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7124178-G-A

154466349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7124178-G-T

154467211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7124624-T-C

154467258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7124660-G-A

154470550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125163-A-G

154470554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125167-T-C

154470577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125187-G-A

154470607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125217-G-A

154470631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125241-T-A

154470679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125292-C-G

154470679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125292-C-T

154470754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125367-T-C

154470957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125569-G-A

154471005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125609-T-C

154471608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7125911-G-C

154471729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126005-T-C

154471759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126035-G-T

154471866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126110-A-G

154471898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126147-A-G

154472075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126358-C-T

154472084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126367-T-C

http://identifiers.org/hco/6/GRCh38#154472243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7126523-C-A

154472243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126523-C-T

154472400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126689-C-T

154472469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7126755-G-A

154474589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7128598-G-A

154474629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7128631-G-A

154474687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7128658-T-C

154474768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7128728-G-A

154474784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7128744-G-C

154474784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7128744-G-T

154475057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7128965-A-G

154475304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7129177-G-A

154475312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7129185-T-C

154475648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7129796-G-A

154475674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7129822-C-T

154475837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7129972-C-T

154475838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7129973-G-A

154475855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7129990-C-G

154476041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7130171-A-G

154478929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7132796-A-G

154478952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7132818-T-C

154479125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7133138-A-G

154479198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7133213-T-A

154479204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7133219-A-G

154479230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7133231-A-T

154479308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7133305-G-A

154479432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7133415-C-T

http://identifiers.org/hco/6/GRCh38#154479597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7133556-C-A

154479828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7133792-T-A

154479874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7133838-T-G

154479916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, undefined
orthologous variants: 7133873-G-A

http://identifiers.org/hco/6/GRCh38#154479968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#7133928-C-A

154480010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7133962-G-A

154480045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7133985-A-T

http://identifiers.org/hco/6/GRCh38#154480158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7134163-A-C

154480158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7134163-A-T

154480166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7134165-C-G

154480200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron_variant, undefined
orthologous variants: 7134198-G-A

154480300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7134270-A-T

154481361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7135670-A-G

154481361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7135670-A-T

154481658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7136023-C-G

154481696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7136060-G-A

154481981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7136335-G-T

154482193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7137087-T-C

154482340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7137218-T-C

154482544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7137392-G-A

http://identifiers.org/hco/6/GRCh38#154482577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7137432-A-C

154482798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7137842-G-A

154485496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7138958-C-T

154485920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7139363-C-T

154485943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7139386-G-C

154486078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7139550-T-C

154486254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7139731-T-A

154487233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7139886-C-T

154488188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7140872-A-G

154488192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7140876-A-G

154488274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7140953-A-G

154488714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141639-T-C

154488731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141656-A-G

154488733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141658-C-T

154488736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141661-T-A

154488787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141702-G-A

http://identifiers.org/hco/6/GRCh38#154488822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7141740-A-C

154489003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141902-G-A

154489005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141904-C-T

154489088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7141981-A-G

154489582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7142141-G-A

154489679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7142231-T-C

154489709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7142261-G-A

154490050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7142544-C-T

154490352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7142847-T-C

154491160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144069-A-T

154491212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144121-A-G

154491251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144162-A-G

154491359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144264-G-T

154491424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144328-T-C

154491624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144519-T-G

154491674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144570-G-A

154491683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7144591-A-G

http://identifiers.org/hco/6/GRCh38#154491753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7144658-A-C

154495203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7146929-A-T

154495253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7146973-A-G

http://identifiers.org/hco/6/GRCh38#154499056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7149757-C-A

http://identifiers.org/hco/6/GRCh38#154499368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7150075-C-A

154499433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7150106-T-A

154499555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7150216-C-T

154500042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7150839-C-T

154500364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7151547-T-C

154500391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7151574-A-G

http://identifiers.org/hco/6/GRCh38#154500996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7152356-A-C

154501069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7152427-G-A

154501091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7152454-T-C

154501145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7152507-T-C

http://identifiers.org/hco/6/GRCh38#154501433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7152758-A-C

154501487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7152820-G-A

154501584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7152910-C-T

154501809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7153138-C-T

154501812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7153141-G-C

154501901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7153890-A-G

154502602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7154926-A-T

154502638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7154960-C-G

154502672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7154986-G-A

154502961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7155231-T-C

154503167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7155429-A-G

154503198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7155457-T-C

154503205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7155464-C-T

154503247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7155503-G-T

154503860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7155812-C-G

154504180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7156383-G-A

154504228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7156455-T-G

154504238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7156464-C-T

154504295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7156524-C-G

154504369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7156596-T-G

154504700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7156903-G-A

154505313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7157332-G-C

154505329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7157351-C-T

154505865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7157544-G-A

154506096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7157760-C-T

154506138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7157807-G-A

154506138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7157807-G-C

154506166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7157843-T-C

http://identifiers.org/hco/6/GRCh38#154506405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7158153-C-A

154506495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7158305-C-G

http://identifiers.org/hco/6/GRCh38#154506554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7158378-C-A

154506554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7158378-C-T

154506726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7158541-A-G

154506936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7158768-G-A

154506947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7158779-G-T

154507109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7158946-G-A

154507151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7158985-C-T

154507224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159058-G-A

154507303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159129-C-T

154507312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159138-G-A

154507494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159305-T-C

154507672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159512-T-G

154507797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159642-A-T

154507904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159742-C-T

154508182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7159975-T-C

154508426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160197-T-C

154508603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160318-T-G

154508698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160399-G-T

154508753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160456-A-G

154508803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160518-C-T

154508985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160682-T-G

154509091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160742-G-T

154509134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160791-G-A

154509324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160952-G-A

154509324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160952-G-C

154509324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7160952-G-T

http://identifiers.org/hco/6/GRCh38#154509733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7161334-C-A

http://identifiers.org/hco/6/GRCh38#154509846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7161438-C-A

154509846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: intron variant
orthologous variants: 7161438-C-T

154510097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 7161666-C-G

154510124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161693-C-T

154510129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161698-C-T

154510146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161715-G-A

http://identifiers.org/hco/6/GRCh38#154510262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7161802-C-A

154510262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161802-C-G

http://identifiers.org/hco/6/GRCh38#154510276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7161816-C-A

154510276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161816-C-G

154510276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161816-C-T

154510290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161831-G-A

154510290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161831-G-T

http://identifiers.org/hco/6/GRCh38#154510329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7161909-C-A

154510329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161909-C-G

154510329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161909-C-T

154510370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161938-G-A

154510370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161938-G-T

154510386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161954-G-A

154510386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7161954-G-T

http://identifiers.org/hco/6/GRCh38#154510436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7162001-C-A

154510460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162029-G-A

154510557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162107-G-A

154510565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162114-G-A

154510565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162114-G-T

154510579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162129-C-T

http://identifiers.org/hco/6/GRCh38#154510624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7162175-C-A

154510624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162175-C-T

154510632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162183-A-G

http://identifiers.org/hco/6/GRCh38#154510640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7162191-C-A

154510640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162191-C-G

154510640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23034
most severe consequence: 5 prime UTR variant
orthologous variants: 7162191-C-T